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Synopsis: This book dives primarily into the perils associated with medical device establishments that fail to comply with US FDA regulatory requirements. It dissects the specific regulatory issue and provides recommendations on how device establishments can comply with regulatory requirements. This is unlike most regulatory books written as Dr. Devine tells the story with an edge and some humor.
About the Author: A well-known and respected medical device industry quality and regulatory expert, Dr. Christopher Joseph Devine is the president and founder of Devine Guidance International, Inc., (DGII) a consulting firm providing regulatory and quality compliance support for the medical device industry. Prior to launching DGII, Dr. Devine spent 14-years with Boston Scientific Corporation working in a variety of quality and regulatory management roles. Additionally, Dr. Devine is the author of Devine Guidance, a weekly blog focusing on quality and regulatory compliance issues facing the medical device industry; and published by the Medical Device Summit, an e-magazine. Furthermore, Dr. Devine has 35-years of combined experience in the fields of quality assurance and regulatory affairs; and is a senior member of the American Society of Quality (ASQ), a member of Regulatory Affairs Professionals Society (RAPS), a member of the Society of Manufacturing Engineers (SME), and a member of the Project Management Institute (PMI). Dr. Devine received his doctorate from Northcentral University, with his doctoral dissertation entitled, “Exploring the Effectiveness of Defensive-Receiving Inspection for Medical Device Manufacturers: A Mixed-Method Study. Finally, Dr. Devine is the author of five books on quality and regulatory compliance published by and available at Amazon.com. Prior to launching his commercial career, Dr. Devine served honorably as a member of the United States Marine Corps.
Title: Devine Guidance - A compilation of Dr. D's ...
Publisher: CreateSpace Independent Publishing Platform
Publication Date: 2015
Binding: Paperback
Book Condition: Good
Edition: 1.
Book Description CreateSpace Independent Publishing Platform, 2015. Condition: Good. 1st Edition. Shows some signs of wear, and may have some markings on the inside. Seller Inventory # GRP90062424
Book Description Createspace Independent Pub, 2015. PAP. Condition: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000. Seller Inventory # IQ-9781517194390
Book Description Createspace Independent Pub, 2015. PAP. Condition: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000. Seller Inventory # IQ-9781517194390
Book Description Createspace Independent Publishing Platform, United States, 2015. Paperback. Condition: New. Language: English. Brand new Book. This book dives primarily into the perils associated with medical device establishments that fail to comply with US FDA regulatory requirements. It dissects the specific regulatory issue and provides recommendations on how device establishments can comply with regulatory requirements. This is unlike most regulatory books written as Dr. Devine tells the story with an edge and some humor. Seller Inventory # APC9781517194390
Book Description CreateSpace Independent Publishing Platform, 2015. Condition: New. This book is printed on demand. Seller Inventory # I-9781517194390
Book Description Createspace Independent Publishing Platform, United States, 2015. Paperback. Condition: New. Language: English. Brand new Book. This book dives primarily into the perils associated with medical device establishments that fail to comply with US FDA regulatory requirements. It dissects the specific regulatory issue and provides recommendations on how device establishments can comply with regulatory requirements. This is unlike most regulatory books written as Dr. Devine tells the story with an edge and some humor. Seller Inventory # APC9781517194390