3700 Courses in Cardiff delivered Online

This course satisfies the supervision requirements in the LAA Standard Contract & covers the key skills needed to ensure compliance with the LAA Contract.

BOHS P304 is designed to give practical guidance on assessing the health risks caused by hazardous substances, in order to meet the requirements of the Control of Substances Hazardous to Health (COSHH) Regulations 2002 for a 'suitable and sufficient' risk assessment.

3 QLS Endorsed Diploma | QLS Hard Copy Certificate Included | Plus 10 CPD Courses | Lifetime Access

10 QLS Endorsed Courses for Conveyancing Paralegal | 10 Endorsed Certificates Included | Life Time Access

Level 2 & 4 Endorsed Diploma | QLS Hard Copy Certificate Included | Plus 5 CPD Courses | Lifetime Access

Level 3, 5 & 7 QLS Endorsed Diploma | QLS Hard Copy Certificate Included | Plus 10 CPD Courses | Lifetime Access

This module aims to develop knowledge and understanding of the role of logistics including an understanding of air, sea, road and rail freight and courier services. It will explore the advantages and disadvantages of using the different modes of transport the world of international trade.

Duration 4 Days 24 CPD hours This course is intended for This course is designed for the aspiring or sitting upper-level manager striving to advance his or her career by learning to apply their existing deep technical knowledge to business problems. In this course, students will learn in-depth content in each of the 5 CCISO Domains Domain 01 - Governance Define, Implement, Manage, and Maintain an Information Security Governance Program Information Security Drivers Establishing an information security management structure Laws/Regulations/Standards as drivers of Organizational Policy/Standards/Procedures Managing an enterprise information security compliance program Risk Management Risk mitigation, risk treatment, and acceptable risk Risk management frameworks NIST Other Frameworks and Guidance (ISO 31000, TARA, OCTAVE, FAIR, COBIT, and ITIL) Risk management plan implementation Ongoing third-party risk management Risk management policies and processes Conclusion Domain 2 - Security Risk Management, Controls, & Audit Management INFORMATION SECURITY CONTROLS COMPLIANCE MANAGEMENT GUIDELINES, GOOD AND BEST PRACTICES AUDIT MANAGEMENT SUMMARY Domain 03 - Security Program Management and Operations PROGRAM MANAGEMENT OPERATIONS MANAGEMENT Summary Domain 04 - Information Security Core Concepts ACCESS CONTROL PHYSICAL SECURITY NETWORK SECURITY ENDPOINT PROTECTION APPLICATION SECURITY ENCRYPTION TECHNOLOGIES VIRTUALIZATION SECURITY CLOUD COMPUTING SECURITY TRANSFORMATIVE TECHNOLOGIES Summary Domain 05 - Strategic Planning, Finance, Procurement and Vendor Management STRATEGIC PLANNING Designing, Developing, and Maintaining an Enterprise Information Security Program Understanding the Enterprise Architecture (EA) FINANCE PROCUREMENT VENDOR MANAGEMENT Summary

Level 5 QLS Endorsed Course | Endorsed Certificate Included | Plus 5 Career Guided Courses | CPD Accredited

Course Overview This course provides a comprehensive introduction to European Medical Device Regulations (EU MDR), offering learners essential knowledge on the regulatory framework that governs medical devices in the European market. It covers the key components of the EU MDR, ensuring compliance with industry standards and regulations, and highlights the importance of quality systems and reporting requirements. Through this course, learners will gain a solid understanding of how to navigate and implement these regulations in their professional practice. This course is ideal for individuals seeking to expand their expertise in medical device regulation and is invaluable for those aiming to work within the medical device industry in Europe. Course Description The "Essentials of European Medical Device Regulations" course delves into the critical aspects of the EU MDR, including its foundational components, regulatory compliance, and the reporting and identification requirements for medical devices. Learners will explore the essential guidelines for ensuring quality systems are in place to maintain product safety and regulatory compliance. With a focus on practical scenarios and real-world applications, this course equips learners with the necessary skills to interpret and implement these regulations effectively. The course is designed for professionals looking to enhance their understanding of medical device regulations within the European market, offering in-depth insights into the key elements of the EU MDR and its impact on the industry. Course Modules Module 01: Overview to European Regulations on Medical Devices Module 02: Essential Components of EU MDR Module 03: Reporting Requirements and Identification Module 04: Quality System in Medical Device Regulation (See full curriculum) Who is this course for? Individuals seeking to understand European medical device regulations. Professionals aiming to enhance their regulatory compliance expertise. Beginners with an interest in the medical device industry. Regulatory professionals in the healthcare and life sciences sector. Career Path Regulatory Affairs Specialist Compliance Manager in the medical device industry Quality Assurance Manager Medical Device Consultant European Market Access Manager