Fundamentals of Medical Device Regulations

This bundle includes the individual medical device subsets from all four Fundamentals of Regulatory Affairs books: US, EU, Canada and International. The subsets cover the entire medical device lifecycle, from product development through postmarketing for all these regions. This book is an excellent resource for finding answers to medical device questions and learning more about the medical device industry. The bundle also is an outstanding study tool for the new RAC (Device) exam.