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Medical Devices and IVDs Training | NSF International

Medical Devices and IVDs Training. NSF International provides regulatory and quality medical devices training courses and professional qualifications. NSF’s training courses are highly interactive and based on real scenarios, helping you meet international requirements throughout the product lifecycle. 

Medical devices training courses to help you stay

We run public training courses. Contact us to learn more. Email: [email protected] Phone: +44 (0)345 086 9000. More than 70% of the top 100 medical device companies were trained by us and our technical trainers have a combined industry and regulatory experience of over 546 years. 

Medical Devices - Training Online 4U

Medical Devices. This is a professionally developed Medical Device training course which incorporates the Medical Devices Regulation (MDR), which became fully applicable in 2021, along with ISO 14155:2020 and Regulatory guidance from the FDA and MHRA. The Medical Devices Regulation (MDR) supersedes the previous Medical Devices Directive (MDD). 

Training and Continuing Education | FDA

Online courses for industry on safety and effectiveness of medical devices and exposure to radiation from medical devices. ORAU Free online courses for … 

Courses - Medical Device HQ

Upon completion, you will receive a course certificate for your training records. Currently available are courses on Risk Management, Design Control, Project Management, Software Development, Safety for Electrical Medical Devices, and Introduction to Working in the Medical Device Industry. 

Medical Device Training | WO | TÜV Rheinland

Modular training courses in the following areas enable you to make sure your products meet complex and diverse international standards, regulations and laws. Curriculums for TÜV certification or university degree equivalents for the medical device industry include: Properly ensure the safety and quality necessary to gain approvals worldwide. 

Medical Device Engineering Certificate Program | UCLA

What you can learn. Medical device engineering that meets FDA and European regulations for safety and quality. Best practices to address requirements for product design and development. Biomaterials and biocompatibility principles in medical device design. Manufacturing processes and techniques for medical devices.