Master Medical Device Development & Us Fda Regulatory Affair
 

Learn Medical Device Regulatory Affairs, Classification, Intended Use, FDA Databases, Premarket Pathways & UDI Labels
What you'll learn
Master key parts of the U.S. medical device regulatory framework, from concept to - market.
Learn how to classify your device, write the intended use and indications for use statements and choose the right premarket pathway .
Gain practical how-to knowledge to enable you plan and execute performance and usability testing that meets FDA expectations as part of eSTAR submissions
Learn the key requirements for medical device labelling, labels, and UDI requirements to stay fully compliant.
Requirements
While prior experience in medical devices is beneficial, the course is structured to provide foundational knowledge and advanced insights. Both beginners and experienced professionals will benefit from the material.
Description
This comprehensive course provides a clear, structured, and practical education on medical device development and U.S. regulatory fundamentals, giving you the tools to navigate medical device development and FDA regulatory affairs with confidence, avoid costly development mistakes, and bring your device to market faster.You will learn how to understand and apply the U.S. regulatory framework from classification and premarket pathways to labelling, UDI requirements, and key parts of the Code of Federal Regulations (CFR).You'll gain the knowledge and strategic insight to take control of your development and regulatory processes.Throughout the course, you'll access real-world examples and practical explanations designed to make the complex world of medical device development look simple, actionable, and directly applicable to your product. You'll also get a peek behind the curtain at proven documentation strategies to help make your FDA submissions clear, organized, and far less stressful. This course is designed for working professionals in the medical device industry, including regulatory affairs associates, quality managers, project managers, design engineers, software developers tc.You'll master essential topics such as: Medical device classification, intended use, indications for use, premarket pathways, FDA product codes, substantial equivalence, and eSTAR submissions. Gain insight into how to determine what performance testing, usability testing, and clinical evaluation will be needed as part of your product development to ensure regulatory clearance or approval. Learn the regulatory requirements around label, labels, and UDI requirements.The course is structured to be completed in about 5 days, making it accessible and efficient for busy professionals. By the end of this course, you will confidently navigate the U.S. medical device regulatory landscape, knowing exactly how to position your device for fast, smooth market release. Eliminate dependency on external consultants, and instead build the expertise in-house.Start your journey today to become a medical device development and regulatory expert - and bring your innovation to market faster than ever.
Who this course is for
Professionals who work in the medical device industry including regulatory affairs associates, quality managers, project managers, design engineers, software/firmware developers or data scientists who wish to learn more about medical device regulatory affairs to aid in product development