Welcome to the new and improved RAPS Regipedia!
Welcome! If you haven't logged in for a while, you may need to reset your password. Please contact us at firstname.lastname@example.org if you need assistance. Please use your EMAIL for your username.
Click here to login if you're a RAPS Member
Recover Your Account Information
RAPS is a place for great networking, making invaluable connections and building a strong community.
More than 22,000 of your colleagues are waiting to connect with you through our global network of chapters and local networking groups and via our award-winning, private online community, Regulatory Exchange.
This book provides a “how to” guide to developing a comprehensive global regulatory strategy for all types of medical devices, including discussions on the development and implementation of global regulatory strategies for medical devices, labeling, clinical, risk management, marketing and postmarketing. The use of standards and regulatory resources for strategy development is discussed as well as need for developing a comprehensive global regulatory process. Other topics include regulation of therapies, devices, combination products and in vitro diagnostic medical devices.
Who Should Read This Book
This book is intended for both the experienced regulatory professional and those entering the profession and designing their own pathway to success in this vastly enriching field. It can be used as a contemporary and integral bookshelf reference in Regulatory Affairs departments of all sizes, as well as a routine textbook in expanding academic curricula in regulatory affairs and quality systems.
More than 25K + of your colleagues are waiting to connect with you through our global network of chapters and local networking groups and via our award-winning, private online community, Regulatory Exchange.