10872 Professional Development courses in Gravesend delivered On Demand

Overview Gain ultimate child safeguarding and risk management skills to become a qualified professional, by taking the all-inclusive Child Safeguarding Officer Training Diploma course.The exclusive Child Safeguarding Officer Training Diploma course covers all the safeguarding fundamentals, including UK child safeguarding laws and regulations, risk assessments, record keeping, and strategies. By attending the course, you'll develop effective communication skills and the personal leadership skills to perform your safeguarding responsibilities properly. You'll gain a solid idea on child psychology that will help you deal with any safeguarding crisis thoroughly. Ensure your professional development by enrolling today! How will I get my certificate? 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. Who is this course for? There is no experience or previous qualifications required for enrolment on this Child Safeguarding Officer Training Diploma. It is available to all students, of all academic backgrounds. Requirements Our Child Safeguarding Officer Training Diploma is fully compatible with PC's, Mac's, Laptop, Tablet and Smartphone devices. This course has been designed to be fully compatible on tablets and smartphones so you can access your course on wifi, 3G or 4G.There is no time limit for completing this course, it can be studied in your own time at your own pace. Career path Having these various qualifications will increase the value in your CV and open you up to multiple sectors such as Business & Management , Admin, Accountancy & Finance, Secretarial & PA, Teaching & Mentoring etc. Course Curriculum 8 sections • 8 lectures • 03:16:00 total length •Introduction to Safeguarding: 00:21:00 •Laws and Guidance: 00:41:00 •Child Abuse: 00:46:00 •Child Sexual Exploitation: 00:34:00 •Responding to Disclosure and Reporting: 00:25:00 •Risks and Risk Assessment: 00:14:00 •: 00:00:00 •Record Keeping: 00:15:00

Overview Enrol in our Quality Management today and build the necessary skills, knowledge and experience to transform your career. The Quality Management could enhance your continuing professional development thus propelling you more towards your dream job. This Quality Management could be your key, if you are interested in a long term career in the field of Quality Management. This Quality Management course consists of a number of easy to digest, in-depth modules which are designed to provide you with detailed knowledge on Quality Management. This Quality Management aims to accompany you through your journey to help you become a master of Quality Management. Learn through a mixture of interactive lessons and online study materials. How will I get my certificate? 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. Who is this course for? There is no experience or previous qualifications required for enrolment on this Quality Management. It is available to all students, of all academic backgrounds. Requirements Our Quality Management is fully compatible with PC's, Mac's, Laptop, Tablet and Smartphone devices. This course has been designed to be fully compatible on tablets and smartphones so you can access your course on wifi, 3G or 4G. There is no time limit for completing this course, it can be studied in your own time at your own pace. Career path Having these various qualifications will increase the value in your CV and open you up to multiple sectors such as Business & Management , Admin, Accountancy & Finance, Secretarial & PA, Teaching & Mentoring etc. Course Curriculum 9 sections • 9 lectures • 02:39:00 total length •Introduction to Quality Management: 00:26:00 •Total Quality Management: 00:17:00 •Quality Measurement and Improvement: 00:25:00 •Quality Control: 00:13:00 •Understanding Customer Expectations and Needs: 00:16:00 •Six Sigma: 00:21:00 •Supply Chain Management: 00:25:00 •Quality Audits: 00:16:00 •Order your Certificate: 00:00:00

Changes to the terms of marketing authorisations for medicinal products, called variations in Europe, must be notified to or approved by the relevant regulatory authorities. Variations include changes to the composition of products, their manufacturing processes, the way they are used, or the indications for which they are authorised. Common approaches are adopted within the European Economic Area to variations to marketing authorisations approved through the Centralised, Decentralised or Mutual Recognition Procedures. Recent legislation has substantially modified the regulatory requirements and extended them to purely national authorisations by member states. This module, which is fully up to date with the new legislation, covers the classification of variations into their several types and the regulatory requirements, guidance and procedures to be followed for each type.

This module outlines the legislative and regulatory context for the development of generic drugs and describes the essential role of the Abbreviated New Drug Application (ANDA) in gaining marketing approval. The use of information in the ‘Orange Book’ is explained, as is the role of patent certification in the application. The importance of establishing bioequivalence between a generic and its reference product is emphasised. The module specifies the content and format requirements for an ANDA submission and describes the FDA’s review and approval process. An outline is given of the Generic Drug User Fee Amendments (GDUFA) and the law’s effects on industry players.

The regulation of biological medicinal products is governed by different laws from those that apply to small-molecule synthetic drugs. Producing faithful copies of therapeutic proteins is more challenging than producing generic drugs. The US legal framework for the licensure of follow-on biologics, and accompanying regulatory guidance from the Food and Drug Administration (FDA), have been established only in recent years.

This module describes the requirements that must be met to obtain licensure of a biological product. Subjects covered include the regulatory context, the content and format of the BLA submission, the review process, and provisions for expedited development and review.

In the medicines and healthcare products industries, computerised systems used in automated manufacturing or laboratory processes to which Good Manufacturing Practice requirements apply need to be validated. This module describes the planning of such validation. It follows the work of a pharmaceutical company's team as they validate the dispensary control system for a new production line.

Manufacturers of medicines and healthcare products must establish, validate and maintain an equipment cleaning programme. This is a regulatory requirement because validated cleaning procedures contribute to the assurance of product purity and safety. This module provides a comprehensive account of equipment cleaning validation requirements and procedures. It follows the work of a pharmaceutical company's validation team as they establish and validate the cleaning program for a new production line.

Before equipment can be used routinely in production, it must first be commissioned and, if necessary, undergo Installation Qualification (IQ). This module describes commissioning and IQ requirements and procedures in the medicines and healthcare products industries. It follows the activities of a typical validation team as they carry out a project for a pharmaceutical company.

Essential to validation is the provision of documented evidence verifying that manufacturing processes will consistently result in products meeting predetermined quality standards. This module describes the purpose, content and use of validation master plans, project validation plans, and other documentation for validation projects in the medicines and healthcare products industries. It describes the activities of a typical validation team as they carry out a project for a pharmaceutical company.