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					<div><p>The Essentials of European Medical Device Regulations course provides a comprehensive overview of the EU MDR, covering everything from classification and reporting to quality systems. You'll learn from experienced professionals and gain the knowledge and skills to successfully ensure your devices comply with the latest regulations and bring them to market.</p><p>In the first section, you will explore the European Medical Device Regulations (EU MDR). Picture yourself gaining a bird's-eye view of the regulatory framework governing European medical devices. As you delve into the essential components of EU MDR in Section 02, envision yourself gaining a profound understanding of device classification, conformity assessment procedures, and the intricacies of clinical evaluations. It's a voyage of discovery that lays the foundation for your expertise.</p><p>Now, picture yourself in Section 03, where you dive into the depths of reporting requirements and identification. You'll acquire the knowledge and confidence to navigate adverse event reporting and product seamlessly recalls. Finally, in Section 04, envision yourself immersed in the world of quality systems within medical device regulation. Gain the skills to ensure product safety and efficacy while adhering to the highest industry standards.</p><p>By completing this course, you'll emerge as a knowledgeable and adept professional ready to conquer the challenges of European Medical Device Regulations. Whether you're a seasoned industry expert seeking to sharpen your skills or a newcomer eager to embark on a rewarding healthcare career, this course is your gateway to success. Join us on this captivating journey and become a master of European medical device compliance.</p><p>Are you ready to embark on a transformative journey through the intricacies of European Medical Device Regulations? Enroll today and unlock the secrets to compliance, quality, and success in the healthcare industry.</p></div>
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			<h2><b> Learning outcome</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Master the fundamentals of European Medical Device Regulations.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Understand the key components of EU MDR, including classification and conformity assessment.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Learn how to navigate reporting requirements and handle identification in compliance with regulations.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Gain proficiency in quality systems integral to medical device regulation.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Acquire the skills needed to ensure product safety and efficacy.</span>
									</li>
						</ul>
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			<h2> <b>Why should I take this course?</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Gain a comprehensive understanding of the EU MDR and its requirements</span>
									</li>
								<li>
											<span>
													</span>
										<span>Learn from experienced professionals who have helped companies comply with the EU MDR</span>
									</li>
								<li>
											<span>
													</span>
										<span>Get the knowledge and skills you need to ensure your devices comply with the latest regulations and bring them to market successfully</span>
									</li>
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										<span>Stay ahead of the curve and avoid costly mistakes</span>
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										<span>Protect the safety and well-being of your patients</span>
									</li>
						</ul>
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			<h2> <b>Career Path</b></h2>		</div>
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											<span>
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										<span>Regulatory Affairs Specialist</span>
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										<span>Quality Assurance Manager</span>
									</li>
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													</span>
										<span>Medical Device Consultant</span>
									</li>
								<li>
											<span>
													</span>
										<span>Clinical Research Associate</span>
									</li>
								<li>
											<span>
													</span>
										<span>Compliance Analyst</span>
									</li>
						</ul>
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			<h2> <b>Requirements</b></h2>		</div>
				</div>
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				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Basic knowledge of medical devices and healthcare regulations.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Access to a computer with internet connectivity.</span>
									</li>
								<li>
											<span>
													</span>
										<span>A desire to excel in the field of medical device regulation.</span>
									</li>
						</ul>
				</div>
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						</div>
			</div>
		</div>
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			</div>
		</section><div>
                            <div>
                                <h2>Course Curriculum</h2>
                            </div>
                            			<div>
				

<div>
<table width="100%">				<tbody><tr>
					<td colspan="4"><strong>Section 01: Overview to European Regulations on Medical Devices</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Overview to European Regulations on Medical Devices</td><td><span>🕐 00:33:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 02: Essential Components of EU MDR</strong></td>
				</tr>
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					<td>▶</td>
					<td>Essential Components of EU MDR</td><td><span>🕐 00:29:00</span></td>
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					<td colspan="4"><strong>Section 03: Reporting Requirements and Identification</strong></td>
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					<td>▶</td>
					<td>Reporting Requirements and Identification</td><td><span>🕐 00:16:00</span></td>
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					<td colspan="4"><strong>Section 04: Quality System in Medical Device Regulation</strong></td>
				</tr>
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					<td>▶</td>
					<td>Quality System in Medical Device Regulation</td><td><span>🕐 00:25:00</span></td>
				</tr>
				</tbody></table></div>

			</div>
		                        </div>

Skill Up

Medical Device Development

Medical Education

Master the European Medical Device Regulations (EU MDR) with this comprehensive course. Gain the knowledge and skills you need to comply with the EU MDR and successfully bring your medical devices to market.

Essentials of European Medical Device Regulations

General Admission

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					<div><p>Gain the skills and credentials to kickstart a successful career and learn from the experts with this step-by-step training course. This European Medical Device Regulations  has been specially designed to help learners gain a good command of European Medical Device Regulations , providing them with a solid foundation of knowledge to become a qualified professional.</p><p>Through this European Medical Device Regulations , you will gain both practical and theoretical understanding of European Medical Device Regulations  that will increase your employability in this field, help you stand out from the competition and boost your earning potential in no time.</p><p>Not only that, but this training includes up-to-date knowledge and techniques that will ensure you have the most in-demand skills to rise to the top of the industry. This qualification is fully accredited, broken down into several manageable modules, ideal for aspiring professionals.</p></div>
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			<h2><b> Learning outcome</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Familiar yourself with the recent development and updates of the relevant industry</span>
									</li>
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											<span>
													</span>
										<span>Know how to use your theoretical knowledge to adapt in any working environment</span>
									</li>
								<li>
											<span>
													</span>
										<span>Get help from our expert tutors anytime you need</span>
									</li>
								<li>
											<span>
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										<span>Access to course contents that are designed and prepared by industry professionals</span>
									</li>
								<li>
											<span>
													</span>
										<span>Study at your convenient time and from wherever you want</span>
									</li>
						</ul>
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			<h2> <b>Why should I take this course?</b></h2>		</div>
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					<ul>
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											<span>
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										<span>Affordable premium-quality E-learning content, you can learn at your own pace.</span>
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										<span>You will receive a completion certificate upon completing the course.</span>
									</li>
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											<span>
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										<span>Internationally recognized Accredited Qualification will boost up your resume.</span>
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										<span>You will learn the researched and proven approach adopted by successful people to transform their careers.</span>
									</li>
								<li>
											<span>
													</span>
										<span>You will be able to incorporate various techniques successfully and understand your customers better.</span>
									</li>
						</ul>
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				<div>
			<h2> <b>Requirements</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>No formal qualifications required, anyone from any academic background can take this course.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Access to a computer or digital device with internet connectivity.</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section><div>
                            <div>
                                <h2>Course Curriculum</h2>
                            </div>
                            			<div>
				

<div>
<table width="100%">				<tbody><tr>
					<td colspan="4"><strong>Module 1: Overview to European Regulations on Medical Devices</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Overview to European Regulations on Medical Devices</td><td><span>🕐 00:45:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Module 2: Essential Components of EU MDR</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Essential Components of EU MDR</td><td><span>🕐 00:42:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Module 3: Reporting Requirements and Identification</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Reporting Requirements and Identification</td><td><span>🕐 00:29:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Module 4: Quality System in Medical Device Regulation</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Quality System in Medical Device Regulation</td><td><span>🕐 00:38:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Mock Exam</strong></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Mock Exam - European Medical Device Regulations</td><td><span>🕐 00:20:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Final Exam</strong></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Final Exam - European Medical Device Regulations</td><td><span>🕐 00:20:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Order Your Certificate</strong></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Order Your Certificate</td><td><span>🕐 00:00:00</span></td>
				</tr>
				</tbody></table></div>

			</div>
		                        </div>

Certificate in Further Education & Training (Cert Ed)

Medical Training

Certificate in Education & Training (CET)

European Computer Driving Licence (ECDL)

Trainers Course

Gain the skills and credentials to kickstart a successful career and learn from the experts with this step-by-step

European Medical Device Regulations

<div data-hook="bgLayers" style="color: rgb(0, 0, 0); box-sizing: border-box;" id="isPasted" fr-original-style=" color: rgb(0, 0, 0);"><div data-mesh-id="comp-lmkyrn781inlineContent-gridContainer" data-testid="mesh-container-content" fr-original-style="" style="box-sizing: border-box;"><div data-testid="richTextElement" fr-original-style="" style="box-sizing: border-box;"><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">This CPD accredited Level 3 course will qualify you as an 1st party internal auditor and a 2nd party supplier auditor. It is a useful precursor to becoming a 3rd party Lead Auditor. The course content has been developed by experienced Lead Auditors.</p><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">It focuses on auditor competencies and best practice for auditing today&rsquo;s industries.</p><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">This course is applicable to any and all industries that need to comply with specified standards and mitigate risk by checking compliance through auditing and inspection. It applies to businesses requiring confidence in their suppliers and to manage their approval through supplier audits. These industries include food, packaging, storage &amp; distribution, pharmaceutical, medical device, automotive etc. It is also applicable to systems and controls applicable to all industries such as health &amp; safety.</p><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">Holders of the qualification will have the knowledge necessary to effectively audit and inspect professionally and ethically for compliance, and to identify risks that require mitigation.&nbsp;</p><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">By the end of this course you will be able to:</p><ul style="color: rgb(var(--color_25)); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));"><li fr-original-style="" style="box-sizing: border-box;"><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">Define purpose, benefit &amp; limitations of audits</p></li><li fr-original-style="" style="box-sizing: border-box;"><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">Use auditing techniques &amp; have required competencies</p></li><li fr-original-style="" style="box-sizing: border-box;"><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">Plan &amp; conduct audits</p></li><li fr-original-style="" style="box-sizing: border-box;"><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">Audit against the appropriate standards</p></li><li fr-original-style="" style="box-sizing: border-box;"><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">Assess and critique sites</p></li></ul><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">A learner will receive a Certificate of Achievement upon successful completion of the exam.</p><p style="color: rgb(var(--color_25)); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(var(--color_25));">&nbsp;This course has been accredited by the CPD Accreditation Office for delivery, structure and content.</p></div></div></div>

This CPD accredited Level 3 course will qualify you as an 1st party internal auditor and a 2nd party supplier auditor. It is a useful precursor to becoming a 3rd party Lead Auditor. The course content has been developed by experienced Lead Auditors.
It focuses on auditor competencies and best practice for auditing today’s industries.
This course is applicable to any and all industries that need to comply with specified standards and mitigate risk by checking compliance through auditing and inspection. It applies to businesses requiring confidence in their suppliers and to manage their approval through supplier audits. These industries include food, packaging, storage & distribution, pharmaceutical, medical device, automotive etc. It is also applicable to systems and controls applicable to all industries such as health & safety.
Holders of the qualification will have the knowledge necessary to effectively audit and inspect professionally and ethically for compliance, and to identify risks that require mitigation. 
By the end of this course you will be able to:
Define purpose, benefit & limitations of audits
Use auditing techniques & have required competencies
Plan & conduct audits
Audit against the appropriate standards
Assess and critique sites
A learner will receive a Certificate of Achievement upon successful completion of the exam.
 This course has been accredited by the CPD Accreditation Office for delivery, structure and content.

Ask Sonia Limited

Food Safety

Internal Auditing

Auditor

CPD accredited Level 3 Effective Auditing & Inspection course. 
Delivered online (Zoom) by a live tutor.
Exam and Certificate fee included in the price.

CPD Accredited Effective Auditing & Inspection Level 3 (1 day)

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			<h2>Overview
</h2>		</div>
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					<p><span>This comprehensive course on </span><b><span>European Medical Device Regulations</span></b> will deepen your understanding on this topic.</p><p><span><span>After successful completion of this course you can acquire the required skills in this sector. This </span><b>European Medical Device Regulations</b> comes with accredited certification, which will enhance your CV and make you worthy in the job market.</span></p><p><span><span>So enrol in this course today to fast track your career ladder.</span></span></p>					</div>
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			<h2>How will I get my certificate?</h2>		</div>
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					<p>You may have to take a quiz or a written test online during or after the course. After successfully completing the course, you will be eligible for the certificate.</p>					</div>
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			<h2>Who is This course for?</h2>		</div>
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					<p><span>There is no experience or previous qualifications required for enrolment on this </span><b><span>European Medical Device Regulations</span></b>. It is available to all students, of all academic backgrounds.</p>					</div>
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			<h2>Requirements</h2>		</div>
				</div>
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								<div>
					<p><span>Our </span><b><span>European Medical Device Regulations</span></b> is fully compatible with PC's, Mac's, Laptop, Tablet and Smartphone devices. This course has been designed to be fully compatible with tablets and smartphones so you can access your course on Wi-Fi, 3G or 4G.</p><p><span><span>There is no time limit for completing this course, it can be studied in your own time at your own pace.</span></span></p>					</div>
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			<h2>Career Path</h2>		</div>
				</div>
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					<p><span>Having these various qualifications will increase the value in your CV and open you up to multiple sectors such as Business &amp; Management, Admin, Accountancy &amp; Finance, Secretarial &amp; PA, Teaching &amp; Mentoring etc.</span></p>					</div>
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					</div> <h3>Course Curriculum</h3><div><p>1 sections • 4 lectures • 02:26:00 total length</p></div><div><div><div><div><div><div><div><p>•Module 1: Overview to European Regulations on Medical Devices: 00:43:00</p></div><div><div><p>•Module 2: Essential Components of EU MDR: 00:40:00</p></div><div><div><p>•Module 3: Reporting Requirements and Identification: 00:27:00</p></div><div><div><p>•Module 4: Quality System in Medical Device Regulation: 00:36:00</p></div></div></div></div></div></div></div></div></div></div>

Apex Learning

Certificate in Emergency Response Ambulance Driving (CERAD)

<div id="course-pricing" fr-original-style="" style="box-sizing: border-box;">
          </div><p id="isPasted" fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Explore the intricacies of European Medical Device Regulations (EU MDR) with our comprehensive course.&nbsp;</span></p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Gain a solid understanding of the European regulations governing medical devices, including the essential components of EU MDR. Learn about reporting requirements, identification processes, and the quality system involved in regulating medical devices.</span></p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Throughout the course, you&#39;ll grasp the significance of adhering to regulatory standards and guidelines for medical devices. With expert guidance and accessible online materials, this course provides a great learning experience for individuals from any academic background.&nbsp;</span></p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Upon completion, receive a CPD certificate to validate your knowledge and enhance your career prospects in regulatory affairs, quality assurance, compliance, and more.</span></p><h2 dir="ltr" id="isPasted" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Learning Outcome of EU Medical Device Regulations</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li id="isPasted" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Learn the overview of European regulations governing medical devices.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Gain insight into the essential components of EU Medical Device Regulations (MDR).</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Understand the reporting requirements and identification processes related to medical devices.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Acquire knowledge about the quality system involved in regulating medical devices.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Learn about compliance with EU MDR standards and guidelines.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Understand the importance of adhering to regulatory requirements for medical devices.</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Key Features of the Course</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">A CPD certificate that is recognised worldwide.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">A great online learning experience.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Interesting and unique online materials and activities.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Expert guidance and support from the field leaders.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Access to the study resources anytime you want.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Friendly and helpful customer service and admin support by email, phone, and chat from Monday through Friday.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Get a year-long access to the course.</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Requirements</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">No prerequisites; suitable for individuals from any academic background.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Accessible course materials from any internet-enabled device.</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">CPD Certificate from Course Gate</span></h2><p dir="ltr" fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">At the successful completion of the course, you can obtain your CPD certificate from us. You can order the PDF certificate for &pound;9 and the hard copy for &pound;15. Also, you can order both PDF and hardcopy certificates for &pound;22.</span></p><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Career path</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li id="isPasted" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Regulatory Affairs Specialist</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Quality Assurance Manager</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Compliance Officer</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Product Safety Manager</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Clinical Affairs Specialist</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Medical Device Consultant</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Course Curriculum</span><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);"><br fr-original-style="" style="box-sizing: border-box;"></span></h2><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><section fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
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</span></div><ul fr-original-style="" style="box-sizing: border-box;"><li id="isPasted" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 01: Overview to European Regulations on Medical Devices</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 02: Essential Components of EU MDR</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 03: Reporting Requirements and Identification</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 04: Quality System in Medical Device Regulation</li></ul></div>

Course Gate

Explore the essentials of European Medical Device Regulations (EU MDR) with our comprehensive course. Gain insights into regulatory requirements, quality systems, and reporting protocols to ensure compliance in the healthcare industry.

Essentials EU Medical Device Regulations

<p>Learn the recent EU medical device regulations and alterations and turn yourself into an asset for the health &amp; care job sector. The starting salary of a medical device consultant is at least £35k annually. So, why wait? Just take the course.</p><p>The Medical Device Regulations (EU) course will help you understand the basic requirements and ideas of the European Medical Devices Regulation. This course will walk you through the important elements of EU MDR, including regulatory developments in the European market, the structure of the regulation, and the partners affected by it. It contains critical information on reporting requirements and identification, as well as an overview of the UK Good Manufacturing Practice Guides.</p><p>Therefore, enrol in our Medical Device Regulations (EU) course to enlarge your knowledge and grab the opportunities that are waiting for you in the near future.</p><p><strong>At the end of the course, learners will be able to:</strong></p><ul><li>Learn more about the EU Medical Devices Regulations and their potential applications</li><li>Discover the most recent alterations to the European market's regulations</li><li>Recognise what EU MDR actually implies in practice</li><li>Possess a thorough understanding of identification and reporting requirements</li><li>Learn in-depth information on how the new rules affect producers, importers, distributors, and EU representatives of medical devices</li><li>Recognise the full procedure for CE marking in accordance with the Medical Devices Regulation (MDR)</li></ul><p><strong>Expert Support</strong></p><p>Dedicated tutor support and 24/7 customer support are available to all students with this premium quality course.</p><p><strong>Key Benefits</strong></p><ul><li>Learning materials of the Design course contain engaging voiceover and visual elements for your comfort.</li><li>Get 24/7 access to all content for a full year.</li><li>Each of our students gets full tutor support on weekdays (Monday to Friday)</li></ul><p><strong>Please note</strong>: This course only gives you the theoretical knowledge that you need to excel in this field. This Essentials of European Medical Device Regulations course doesn't entitle you to practise as a professional in this specific field.</p><p><strong>COURSE CURRICULUM</strong></p><p><strong>Essentials of European Medical Device Regulations</strong></p><ul><li>Module 1: Overview to European Regulations on Medical Devices</li><li>Module 2: Essential Components of EU MDR</li><li>Module 3: Reporting Requirements and Identification</li><li>Module 4: Quality System in Medical Device Regulation</li></ul><p><strong>Meet the Accreditation</strong></p><p><strong>The CPD Certification Service (CPD UK</strong>) assures the <strong>Essentials of European Medical Device Regulations</strong> course training and learning activities are relevant, reliable, and upto date.</p><p><strong>Course Assessment </strong></p><p>To simplify the procedure of evaluation and accreditation for learners, we provide an automated assessment system. Upon completion of an online module, you will immediately be given access to a specifically crafted MCQ test. The results will be evaluated instantly, and the score will be displayed for your perusal. For each test, the pass mark will be set to 60%.</p><p>When all tests have been successfully passed, you will be able to order a certificate endorsed by the Quality Licence Scheme.</p><p><strong>Exam &amp; Retakes:</strong></p><p>It is to inform our learners that the initial exam for this online course is provided at no additional cost. In the event of needing a retake, a nominal fee of £9.99 will be applicable.</p><p><strong>Certification</strong></p><p>Upon successful completion of the assessment procedure, learners can obtain their certification by placing an order and remitting a fee of £9 for PDF Certificate and £15 for the Hardcopy Certificate within the UK ( An additional £10 postal charge will be applicable for international delivery).</p><h2>
        
        <div>CPD</div>
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                                        10 CPD hours / points
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                                            Accredited by The CPD Certification Service
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        <div>Who is this course for?</div>
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                            <ul><li>Senior Regulatory Affairs Specialist</li><li>Sales Representative CP</li><li>Medical Writer</li><li>Quality System Engineer</li></ul>
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        <div>Requirements</div>
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                            <p>This Medical Device Regulations (EU) course is open to all, with no formal entry requirements.</p>
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        <div>Career path</div>
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                            <ul><li>Medical Secretary (£17,500 to £24,000) per annum</li><li>Medical illustrator (£25,654 to £39,026) per annum</li><li>Regulatory Medical Device Engineer (£50,000 to £60,000) per annum</li><li>Regulatory Medical Device Consultant (£50,000 to £60,000) per annum</li><li>Midwife - Medical Device Trainer (£35,000 to £45,000) per annum</li></ul>
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One Education

Medical Device Regulations (EU) Course

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							<p><span>By enroling in Essentials of European Medical Device Regulations, you can kickstart your vibrant career and strengthen your profound knowledge. You can learn everything you need to know about the topic.</span></p><p><span>The Essentials of European Medical Device Regulations course includes all of the most recent information to keep you abreast of the employment market and prepare you for your future. The curriculum for this excellent Essentials of European Medical Device Regulations course includes modules at all skill levels, from beginner to expert. You will have the productivity necessary to succeed in your organisation once you have completed our Essentials of European Medical Device Regulations Program.</span></p><p><span>So enrol in our Essentials of European Medical Device Regulations course right away if you're keen to envision yourself in a rewarding career.</span></p>						</div>
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							<p><span>Enroling in this Essentials of European Medical Device Regulations course can improve your Essentials of European Medical Device Regulations perspective, regardless of your skill levels in the Essentials of European Medical Device Regulations topics you want to master. If you're already a Essentials of European Medical Device Regulations expert, this peek under the hood will provide you with suggestions for accelerating your learning, including advanced Essentials of European Medical Device Regulations insights that will help you make the most of your time. This Essentials of European Medical Device Regulations course will act as a guide for you if you've ever wished to excel at Essentials of European Medical Device Regulations.</span></p>						</div>
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							<ul><li><span>After successfully completing the Essentials of European Medical Device Regulations Course, you will receive a </span><b>FREE PDF Certificate </b><span>as evidence of your newly acquired abilities.</span></li><li><span>Lifetime access to the whole collection of Essentials of European Medical Device Regulations learning materials.</span></li><li><span>Online test with immediate results</span></li><li><span>Enroling in the course has no additional cost.</span></li><li><span>You can study and complete the Essentials of European Medical Device Regulations course at your own pace.</span></li><li><span>Study for the Essentials of European Medical Device Regulations course using any internet-connected device, such as a computer, tablet, or mobile device.</span></li></ul>						</div>
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							<p><span>This Essentials of European Medical Device Regulations course is a great place to start if you're looking to start a new career in Essentials of European Medical Device Regulations field. This training is for anyone interested in gaining in-demand Essentials of European Medical Device Regulations proficiency to help launch a career or their business aptitude. </span></p>						</div>
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							<p><span>The Essentials of European Medical Device Regulations course requires no prior degree or experience. All you require is English proficiency, numeracy literacy and a gadget with stable internet connection. Learn and train for a prosperous career in the thriving and fast-growing industry of Essentials of European Medical Device Regulations, without any fuss.</span></p>						</div>
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							<p><span>This Essentials of European Medical Device Regulations training will assist you develop your Essentials of European Medical Device Regulations ability, establish a personal brand, and present a portfolio of relevant talents. It will help you articulate a  Essentials of European Medical Device Regulations professional story and personalise your path to a new career. Furthermore, developing this Essentials of European Medical Device Regulations skillset can lead to numerous opportunities for high-paying jobs in a variety of fields.</span></p>						</div>
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					<td>Module 1: Overview to European Regulations on Medical Devices</td>
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NextGen Learning

Essentials of European Medical Device Regulations Course

<p>Delve into the intricacies of European medical device regulatory frameworks with our comprehensive course, '<strong>Essentials of European Medical Device Regulations</strong>.' This meticulously structured program provides an in-depth exploration of the critical components and legislative requirements necessary for navigating the complex landscape of medical device regulations in Europe. The first module introduces the foundational aspects of the European regulations, setting the stage for a deeper understanding of the legal and procedural elements that govern this sector. As the course progresses, participants will gain a thorough grasp of the Essential Components of EU MDR (Module 2), the pivotal aspects of Reporting Requirements and Identification (Module 3), and the integral role of Quality Systems in medical device regulation (Module 4). This course is meticulously designed to cater to the needs of professionals seeking a robust understanding of the regulatory environment, ensuring they are well-equipped to adhere to and implement these critical regulations.</p>
<p><strong>Learning Outcomes</strong></p>
<ul>
<li>Acquire a solid foundation in the basic principles and framework of European regulations on medical devices.</li>
<li>Understand the key elements of the EU Medical Device Regulation (MDR) and their application in the industry.</li>
<li>Gain insights into the specific requirements for reporting and identification within the European regulatory context.</li>
<li>Learn about the implementation and management of quality systems in compliance with medical device regulations.</li>
<li>Develop the ability to interpret and apply regulatory guidelines in professional settings, enhancing compliance and operational efficiency.</li>
</ul>
<h3><b>Why choose this Essentials of European Medical Device Regulations<span> course</span>?</b></h3>
<ol>
<li>Unlimited access to the course for a lifetime.</li>
<li>Opportunity to earn a certificate accredited by the <b>CPD Quality Standards</b> and <b>CIQ </b>after completing this course.</li>
<li>Structured lesson planning in line with industry standards.</li>
<li>Immerse yourself in innovative and captivating course materials and activities.</li>
<li>Assessments designed to evaluate advanced cognitive abilities and skill proficiency.</li>
<li>Flexibility to complete the Course at your own pace, on your own schedule.</li>
<li>Receive full tutor support throughout the week, from Monday to Friday, to enhance your learning experience.</li>
<li>Unlock career resources for CV improvement, interview readiness, and job success.</li>
</ol>
<h3><b>Who is this Essentials of European Medical Device Regulations<span> </span></b><b><span>course </span></b><b>for?</b></h3>
<ul>
<li>Professionals in the medical device industry seeking to deepen their understanding of EU regulations.</li>
<li>Regulatory affairs specialists aiming to stay updated with the latest European legislative changes.</li>
<li>Quality assurance personnel in the healthcare sector requiring knowledge of regulatory compliance.</li>
<li>Medical device manufacturers and distributors needing to align their products with EU standards.</li>
<li>Healthcare consultants and advisors focusing on European medical device regulatory frameworks.</li>
</ul>
<h3><b>Career path</b></h3>
<ul>
<li><strong>Regulatory Affairs Manager</strong>: £40,000 - £60,000</li>
<li><strong>Quality Assurance Specialist</strong>: £35,000 - £50,000</li>
<li><strong>Compliance Officer</strong>: £30,000 - £45,000</li>
<li><strong>Product Development Engineer</strong>: £33,000 - £55,000</li>
<li><strong>Healthcare Consultant</strong>: £45,000 - £70,000</li>
<li><strong>Medical Device Auditor</strong>: £37,000 - £53,000</li>
</ul>
<h3><b>Prerequisites</b></h3>
<p><span>This </span><b>Essentials of European Medical Device Regulations</b><span> does not require you to have any prior qualifications or experience. You can just enrol and start learning. This </span><span>course</span><span> was made by professionals and it is compatible with all PC's, Mac's, tablets and smartphones. You will be able to access the course from anywhere at any time as long as you have a good enough internet connection.</span></p>
<h3><b>Certification</b></h3>
<p><span>After studying the course materials, there will be a written assignment test which you can take at the end of the course. After successfully passing the test you will be able to claim the pdf certificate for £4.99 Original Hard Copy certificates need to be ordered at an additional cost of £8.</span></p><div>
				<h3>
	<span>Course Curriculum</span>
</h3>

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<table width="100%">				<tbody><tr>
					<td colspan="4">Module 1: Overview to European Regulations on Medical Devices</td>
				</tr>
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					<td><i></i></td>
					<td>Overview to European Regulations on Medical Devices</td>
					<td> </td>
					<td><span><i></i> 00:43:00</span></td>
				</tr>
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					<td colspan="4">Module 2: Essential Components of EU MDR</td>
				</tr>
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					<td><i></i></td>
					<td>Essential Components of EU MDR</td>
					<td> </td>
					<td><span><i></i> 00:40:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 3: Reporting Requirements and Identification</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Reporting Requirements and Identification</td>
					<td> </td>
					<td><span><i></i> 00:27:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 4: Quality System in Medical Device Regulation</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Quality System in Medical Device Regulation</td>
					<td> </td>
					<td><span><i></i> 00:36:00</span></td>
				</tr>
				</tbody></table></div>

			</div>

Studyhub UK

MRCS

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				<p><span>Register on the Essentials of European Medical Device Regulations today and build the experience, skills and knowledge you need to enhance your professional development and work towards your dream job. Study this course through online learning and take the first steps towards a long-term career.</span></p><p><span>The course consists of a number of easy to digest, in-depth modules, designed to provide you with a detailed, expert level of knowledge. Learn through a mixture of instructional video lessons and online study materials.</span></p><p><span>Receive online tutor support as you study the course, to ensure you are supported every step of the way. Get an e-certificate as proof of your course completion.</span></p><p><span>The Essentials of European Medical Device Regulations is incredibly great value and allows you to study at your own pace. Access the course modules from any internet-enabled device, including computers, tablet, and smartphones.</span></p><p><span>The course is designed to increase your employability and equip you with everything you need to be a success. Enrol on the now and start learning instantly!</span></p><h5><b>What You Get With The Essentials of European Medical Device Regulations </b></h5><ul><li><span>Receive a e-certificate upon successful completion of the course</span></li><li><span>Get taught by experienced, professional instructors</span></li><li><span>Study at a time and pace that suits your learning style</span></li><li><span>Get instant feedback on assessments </span></li><li><span>24/7 help and advice via email or live chat</span></li><li><span>Get full tutor support on weekdays (Monday to Friday)</span></li></ul>					</div>
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			<h2>Course Design</h2>		</div>
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				<div id="course-home"><div><p><span>The course is delivered through our online learning platform, accessible through any internet-connected device. There are no formal deadlines or teaching schedules, meaning you are free to study the course at your own pace.</span></p><p><span>You are taught through a combination of</span></p><ul><li><span>Video lessons</span></li><li><span>Online study materials</span></li></ul></div></div>					</div>
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			<h2>Certification</h2>		</div>
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				<p><span>Upon successful completion of the course, you will be able to obtain your course completion e-certificate free of cost. Print copy by post is also available at an additional cost of £9.99 and PDF Certificate at £4.99.</span></p>					</div>
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			<h2>Who Is This Course For:</h2>		</div>
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				<p><span>The course is ideal for those who already work in this sector or are an aspiring professional. This course is designed to enhance your expertise and boost your CV. Learn key skills and gain a professional qualification to prove your newly-acquired knowledge.</span></p>					</div>
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			<h2>Requirements:</h2>		</div>
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				<p><span>The online training is open to all students and has no formal entry requirements. To study the Essentials of European Medical Device Regulations, all your need is a passion for learning, a good understanding of English, numeracy, and IT skills. You must also be over the age of 16.</span></p>					</div>
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				<h3>Course Content</h3>

<div id="course_curriculum">
<table width="100%">				<tbody><tr>
					<td colspan="4">Essentials of European Medical Device Regulations</td>
				</tr>
								<tr>
					<td colspan="4">Module 1: Overview to European Regulations on Medical Devices	</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Overview to European Regulations on Medical Devices</td>
					<td> </td>
					<td><span><i></i> 00:45:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 2: Essential Components of EU MDR	</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Essential Components of EU MDR</td>
					<td> </td>
					<td><span><i></i> 00:42:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 3: Reporting Requirements and Identification	</td>
				</tr>
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					<td><i></i></td>
					<td>Reporting Requirements and Identification</td>
					<td> </td>
					<td><span><i></i> 00:29:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 4: Quality System in Medical Device Regulation	</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Quality System in Medical Device Regulation</td>
					<td> </td>
					<td><span><i></i> 00:38:00</span></td>
				</tr>
				</tbody></table></div>

			</div>
			<h2>Frequently Asked Questions</h2>
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                                <span>
                                    Are there any prerequisites for taking the course?
                                </span>
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                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        There are no specific prerequisites for this course, nor
                                        are there any formal entry requirements. All you need is
                                        an internet connection, a good understanding of English
                                        and a passion for learning for this course.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
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                                <span>
                                    Can I access the course at any time, or is there a set
                                    schedule?
                                </span>
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                                    <span></span>
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                                    <p>
                                        You have the flexibility to access the course at any time
                                        that suits your schedule. Our courses are self-paced,
                                        allowing you to study at your own pace and convenience.
                                    </p>
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                                    How long will I have access to the course?
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                                        For this course, you will have access to the course
                                        materials for 1 year only. This means you can review the
                                        content as often as you like within the year, even after
                                        you've completed the course. However, if you buy Lifetime
                                        Access for the course, you will be able to access the
                                        course for a lifetime.
                                    </p>
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                                    Is there a certificate of completion provided after
                                    completing the course?
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                                        Yes, upon successfully completing the course, you will
                                        receive a certificate of completion. This certificate can
                                        be a valuable addition to your professional portfolio and
                                        can be shared on your various social networks.
                                    </p>
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                            </div>
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                                <span>
                                    Can I switch courses or get a refund if I'm not satisfied
                                    with the course?
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                                    <p>
                                        We want you to have a positive learning experience. If
                                        you're not satisfied with the course, you can request a
                                        course transfer or refund within 14 days of the initial
                                        purchase.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
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                                <span>
                                    How do I track my progress in the course?
                                </span>
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                                    <span></span>
                                </div>
                            </div>
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                                    <p>
                                        Our platform provides tracking tools and progress
                                        indicators for each course. You can monitor your progress,
                                        completed lessons, and assessments through your learner
                                        dashboard for the course.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    What if I have technical issues or difficulties with the
                                    course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
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                                    <p>
                                        If you encounter technical issues or content-related
                                        difficulties with the course, our support team is
                                        available to assist you. You can reach out to them for
                                        prompt resolution.
                                    </p>
                                </div>
                            </div>
                        </div>

Janets

<p>Unlock the secrets to navigating the intricate landscape of European medical device regulations with our comprehensive course. Designed for those who seek mastery in understanding and applying the latest EU standards, this course is your gateway to compliance excellence. Dive deep into the regulatory environment, where you'll explore the essential components that govern the medical device industry in Europe. Learn how to seamlessly integrate these regulations into your practice, ensuring your products meet the highest standards of safety and efficacy.</p><p><strong>Key Features:</strong></p><ul><li>CPD Certified </li><li>Free Certificate from Reed</li><li>CIQ Approved</li><li>Developed by Specialist</li><li>Lifetime Access </li></ul><p>Discover the nuances of reporting requirements and identification processes, critical for maintaining transparency and accountability. Our expertly curated content guides you through establishing a robust quality system, pivotal for regulatory success. Equip yourself with the knowledge to confidently manage regulatory submissions and navigate quality audits with ease. Join a community of like-minded professionals and elevate your regulatory expertise, ensuring your organisation stays ahead in the competitive medical device market. Enrol now to transform your approach to European medical device regulations and lead with confidence in a compliant and efficient manner.</p><p><strong>Course Curriculum</strong></p><ul><li>Module 01: Overview to European Regulations on Medical Devices</li><li>Module 02: Essential Components of EU MDR</li><li>Module 03: Reporting Requirements and Identification</li><li>Module 04: Quality System in Medical Device Regulation</li></ul><p><strong>Learning Outcomes:</strong></p><ul><li>Understand the core elements of European medical device regulations.</li><li>Identify key components of EU Medical Device Regulation (MDR).</li><li>Master reporting requirements and device identification processes.</li><li>Implement quality systems in medical device regulation.</li><li>Analyse essential EU MDR regulatory requirements.</li><li>Navigate the complexities of EU medical device compliance.</li></ul><h2>
        
        <div>CPD</div>
    </h2>

                        <div id="cpd">
                            <div>
                                <div>
                                    <div>
                                        10 CPD hours / points
                                    </div>
                                        <div>
                                            Accredited by CPD Quality Standards
                                        </div>
                                </div>
                            </div>
                        </div><li>
                                        <h3>
                                            
                                                Essential Components of European Medical Device Regulations <span>1:45:07</span>
                                                <span></span>
                                            
                                        </h3>
                                        <ul id="section1">
                                                <li>
                                                    <span>1: Module 01: Overview to European Regulations on Medical Devices		</span>

                                                    <span>33:17</span>

                                                        
                                                                                                                                                                                                            </li>
                                                <li>
                                                    <span>2: Module 02: Essential Components of EU MDR		</span>

                                                    <span>29:12</span>

                                                        
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                                                    <span>3: Module 03: Reporting Requirements and Identification		</span>

                                                    <span>16:21</span>

                                                        
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                                                <li>
                                                    <span>4: Module 04: Quality System in Medical Device Regulation</span>

                                                    <span>25:17</span>

                                                        
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                                                <li>
                                                    <span>5: CPD Certificate - Free</span>

                                                    <span>01:00</span>

                                                                                                                                                                
                                                                                                    </li>
                                        </ul>
                                    </li><h2>
        
        <div>Who is this course for?</div>
    </h2>

                        <div id="who_is_this_course_for">
                            <ul><li>Regulatory affairs specialists in the medical device industry.</li><li>Quality assurance professionals in healthcare.</li><li>Compliance officers in medical device companies.</li><li>Medical device product managers.</li><li>Legal advisors in healthcare regulation.</li></ul>
                        </div><h2>
        
        <div>Career path</div>
    </h2>

                        <div id="career_path">
                            <ul><li>Regulatory Affairs Specialist</li><li>Quality Assurance Manager</li><li>Compliance Officer</li><li>Medical Device Consultant</li><li>Product Manager</li><li>Regulatory Affairs Associate</li></ul>
                        </div><h2>
        
        <div>Certificates</div>
    </h2>

                        <div id="optional_extras">
                                    <h4>Digital certificate</h4>
        <p>
            Digital certificate -
            Included
        </p>
        <h4>Reed Courses Certificate of Completion</h4>
        <p>
            Digital certificate -
            Included
        </p>
            <div><p>Will be downloadable when all lectures have been completed.</p></div>

                        </div>

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