Online courses for industry on safety and effectiveness of medical devices and exposure to radiation from medical devices. Free online courses for state, local, and tribal regulatory partners....

Become adept in the EU Medical Device Regulation (MDR) and CE marking. Our training will help you and your organization learn the key requirements, concepts, and processes to comply with the EU MDR 2017/745 and the CE marking.

The Regulatory Affairs Certificate: Medical Devices provides a cost-effective, convenient option that will equip you or your organizational team with the tools and knowledge needed to …

NSF provides regulatory and quality medical devices training courses and professional qualifications. Based on timely, real-world experience rooted in industry best practices and regulator insights, NSF’s interactive training helps you meet international requirements throughout the product lifecycle.

Understand the Medical Device Single Audit Program (MDSAP) and its function in the United States; Identify the pre-market regulations and pathways to market for medical devices in the United States; Distinguish how the Food and Drug …

NSF’s training courses give you tools to ensure your product complies with international standards and regulations. Our diverse training programs teach you how to implement and apply global guidelines through all stages of the product lifecycle.

Learn about regulatory requirements, design processes, and testing methods. Transform you career with Coursera's online Medical Device courses. Enroll for free, earn a certificate, and build job-ready skills on your schedule. Join today!

The Certified Medical Device Compliance Professional (CMDCP) program gives you the compliance training needed to advance your career and satisfy regulatory training requirements.

This comprehensive training package of ten courses is aimed at helping medical device companies gain a thorough understanding of the top 10 regulations that they should comply with.

Medical device compliance training will provide the industry best practices for preventing device recalls and will help you to prepare for regulatory inspection, including how to do follow-up with the regulatory agencies.