"AN OVERVIEW OF THE FDA MEDICAL DEVICE REGULATIONS"

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Book	Author(s)	Year	Publisher
Medical Device Regulations		2022	Academic Press
An Overview of FDA Regulated Products	Eunjoo Pacifici and Susan Bain	2018	Academic Press
FDA and Intellectual Property Strategies for Medical Device Technologies	Gerald B. Halt; John C. Donch; Amber R. Stiles; Lisa Jenkins VanLuvanee; Brandon R. Theiss; Dana L. Blue	1st ed. 2019	Springer International Publishing
Medical Device Guidelines and Regulations Handbook	Prakash Srinivasan Timiri Shanmugam; Pugazhenthan Thangaraju; Nandakumar Palani; Thamizharasan Sampath	1st ed. 2022	Springer International Publishing
Medical device technologies: a systems based overview using engineering standards /	Baura, Gail D.	©2012.	Elsevier/Academic Press,
Medical Device Register: The Official Directory of Medical Manufacturers (Medical Device Register (United States))	Mdr	January 2007	Grey House Publishing
Medical Device Design	Ogrodnik; Peter	2013	Academic Press
Medical Device Technologies	Gail Baura	2012	Academic Press
Medical device manufacturing /	Jackson, Mark J.; Davim, Paulo.	c2012.	Nova Science Publishers,
Medical Device Regulatory Practices: An International Perspective	Val Theisz	2015	Routledge
Duke chief medical residents: an overview /	Greenfield, Joseph C.,	[2005], ©2005.	Carolina Academic Press,
Code of federal regulations 21: parts 807, 812, and 814: medical device approval	Interpharm	2003	CRC Press
Handbook of Medical Device Design	Richard C. Fries	2001	Routledge
Handbook of Medical Device Design	Richard C. Fries	2001	Routledge
Medical Device Amendments of 1992	United States	1992	U.S. G.P.O.;Supt. of Docs., U.S. G.P.O., distributor]
Preventing Medical Device Recalls	Dev Raheja	2014	Routledge
Medical Device Packaging Handbook	Harold A. Hughes; Max Sherman	1998	Routledge
Medical device register, 2010	Grey House Publishing, Inc	2009	Grey House Pub.
The Effect of FDA Regulations (GRAS) on Plant Breeding and Processing	Crop Science Society of America \| Hanson, C. H.	2020	John Wiley & Sons
An Act to Repeal an Unnecessary Medical Device Reporting Requirement.	United States	1996	U.S. G.P.O.;Supt. of Docs., U.S. G.P.O., distributor
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Showing 1 to 20 of 100 entries

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Chapter	Author(s)	Book	Book Authors	Year	Publisher
AN OVERVIEW OF THE FDA MEDICAL DEVICE REGULATIONS	David A. Jacobs; James A. Connor; Paul M. Chetham; A. Kent Harnois; Maurice R. Brodeur; David M. Flynn; Peter W. Kotilainan; Robert A. Peura	Bioengineering: Proceedings of the Eighth Northeast Conference	Igor Paul	1980	Pergamon
Australian Medical Device Regulations: An Overview	Petahn McKenna	Medical Affairs: An International Handbook for Medical Devices and Healthcare Products	Jack Wong; Raymond K. Y. Tong	2022	Routledge
Australian medical device regulations: An overview	Petahn McKenna	Handbook of Medical Device Regulatory Affairs in Asia: Second Edition	Jack Wong; Raymond K. Y. Tong	2018	Routledge
Australian Medical Device Regulations: An Overview		Handbook of Medical Device Regulatory Affairs in Asia	Jack Wong; Raymond Tong Kaiyu	2013	Routledge
FDA Medical Device Regulation		FDA Regulatory Affairs: Third Edition	David Mantus; Douglas J. Pisano	2014	Routledge
FDA Medical Device Regulation	Barry Sall	FDA Regulatory Affairs: A Guide for Prescription Drugs, Medical Devices, and Biologics	Douglas J. Pisano; David S. Mantus	2008	Routledge
Medical device regulations	Mounika Gudeppu; Swaroop Sawant; Chella Ganapathy Chockalingam; Prakash Srinivasan Timiri Shanmugam	Trends in Development of Medical Devices	Logesh Chokkalingam; Prakash Srinivasan Timiri Shanmugam andPramila Bakthavachalam	2020	Academic Press
7. FDA Medical Device Regulation	Barry Sall	FDA regulatory affairs: a guide for prescription drugs, medical devices, and biologics /	Pisano, Douglas J.; Mantus, David.	[2004], ©2004.	CRC Press,
FDA Regulations	Richard C. Fries	Handbook of Medical Device Design	Richard C. Fries	2001	Routledge
FDA Regulations		Diagnostic Pathology: Molecular Oncology		2016	Elsevier
FDA regulations		Biomedical engineering entrepreneurship	Jen-shih Lee	2010	World Scientific
FDA Regulations		Frying technology and practices	Monoj K. Gupta, Kathleen Warner, Pamela J. White	2004	AOCS Press
Directives, Regulations and Standards for the Medical Device Industry: An Overview	C.J. Knill; J.F. Kennedy	Medical and Healthcare Textiles	S.C. Anand; J.F. Kennedy; M. Miraftab and S. Rajendran	2010	Woodhead Publishing
Understanding medical foods under FDA regulations	Claudia A. Lewis; Michelle C. Jackson; Jordan R. Bailey	Nutraceutical and Functional Food Regulations in the United States and around the World (Third Edition)	Debasis Bagchi	2019	Academic Press
Understanding Medical Foods under FDA Regulations	Claudia A. Lewis; Michelle C. Jackson	Nutraceutical and Functional Food Regulations in the United States and Around the World (Second Edition)	Debasis Bagchi	2014	Academic Press
FDA History and Relevant Non-Device Regulations	Paul H. King; Richard C. Fries; Arthur T. Johnson	Design of Biomedical Devices and Systems	Paul H. King; Richard C. Fries; Arthur T. Johnson	2018	Routledge
Medical Device Regulations, Combination Product, Study Committees, and FDA-Sponsor Meetings		Design, Execution, and Management of Medical Device Clinical Trials	Salah Abdel-Aleem PhD,	2009	John Wiley & Sons
Medical device regulations in China	C. Shan; M. Liu	Biocompatibility and Performance of Medical Devices (Second Edition)	Jean-Pierre Boutrand	2019	Woodhead Publishing
Medical device regulations in China	S. Likui	Biocompatibility and Performance of Medical Devices	J-P. Boutrand	2012	Woodhead Publishing
Overview of medical device processing	Muhammad Sadeque; Saravana Kumar Balachandran	Trends in Development of Medical Devices	Logesh Chokkalingam; Prakash Srinivasan Timiri Shanmugam andPramila Bakthavachalam	2020	Academic Press
Chapter	Author(s)	Book	Book Authors	Year	Publisher

Showing 1 to 20 of 100 entries

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