FDA Regulatory Affairs is a roadmap to prescription drug, biologics, and medical device development in the United States. Written in plain English, the concise and jargon-free text demystifies the inner workings of the US Food and Drug Administration (FDA) and facilitates an understanding of how the agency operates with respect to compliance and product approval, including clinical trial exemptions, fast track status, advisory committee procedures, and more.
The Third Edition of this highly successful publication:
Co-edited by an industry leader (Mantus) and a respected academic (Pisano), FDA Regulatory Affairs, Third Edition delivers a compilation of the selected US laws and regulations as well as a straightforward commentary on the FDA product approval process that’s broadly useful to both business and academia.
"This book covers the myriad of topics related to the development and marketing of all types of drugs and devices regulated by the U.S. Food and Drug Administration. The book discusses not only the relevant regulations, but also the administrative processes that sponsors must deal with in getting their products approved for marketing. … This book covers many of the important issues in enough depth to answer basic questions related to the components of an IND (investigational new drug) and an NDA (new drug application), as well as IDE (investigational device exemption) and 510k applications. … This book fulfills a unique need for those seeking a book for a course in drug and device development or for those in the industry who seek information outside of their area of expertise."
—Michael R. Jacobs, BS, PharmD, Temple University School of Pharmacy, in Doody's Book Reviews
Overview of FDA and Drug Development
Josephine C. Babiarz and Douglas Pisano
What Is an IND?
Michael R. Hamrell
The New Drug Application
Charles Monahan and Josephine C. Babiarz
Meetings with the FDA
Alberto Grignolo and Sally Choe
FDA Medical Device Regulation
A Primer of Drug/Device Law: What Is the Law and How Do I Find It?
Josephine C. Babiarz
The Development of Orphan Drugs
Scott N. Freeman
CMC Sections of Regulatory Filings and CMC Regulatory Compliance during Investigational and Postapproval Stages
Prabu Nambiar, Steven R. Koepke, and Kevin Swiss
Overview of the GxPs for the Regulatory Professional
Bob Buckley, Robert Blanks, Kimberly J. White, and Tonya White-Salters
FDA Regulation of the Advertising and Promotion of Prescription Drugs, Biologics, and Medical Devices
Karen L. Drake, Esq.
The Practice of Regulatory Affairs
David S. Mantus
FDA Advisory Committees
Christina A. McCarthy and David S. Mantus
Regulation of Combination Products in the United States
John Barlow Weiner, Esq.