The CFR Title 21 Part 820 Memory Jogger – GOAL/QPC
Por um escritor misterioso
Last updated 31 outubro 2024
Check out the Table of Contents and selected pages at the link below.
The CFR Title 21 Part 820 Memory Jogger is an exact copy of the US Government Code of Federal Regulations U.S. Food & Drug Administration Title 21 Food and Drugs, Chapter I - Food and Drug Administration Department of Health and Human Services, Subchapter H Medical Devices, Part 820, Quality System Regulation, Medical Devices, Current Good Manufacturing Practice, April 1, 2021 Edition.
The pocket size (3.5 x 5.5) is easy to carry around and the spiral binding makes for easy reading as it will stay flat and open on a desk etc. for reviewing. The book is available for individual purchase or in a four pack or six pack at a 33% discount.
GOAL/QPC is also offering the purchaser of this book one year of free access to the digital version of this CFR Title 21 Part 820 Memory Jogger. With just a few clicks on your phone, tablet, or computer you can read through chapters or jump right to the section you are looking for with ease. You can also easily resize the text to suit your viewing style, make notes, and add links to examples, either private or across a group. Never be without your CFR Title 21 Part 820 Memory Jogger again!
GOAL/QPC can also customize this CFR Title 21 Part 820 Memory Jogger for you for free with a minimum purchase order of 25 copies. Our design team can add your logo to the cover, redesign the covers to suit your company branding, add messages from your CEO to the inside cover, add your Quality Policy to back cover, etc.
ISBN Pocket size (3.5 x 5.5): 978-1-57681-245-7
ISBN Pocket size (3.5 x 5.5 4 Pack): 978-1-57681-251-8
ISBN Pocket size (3.5 x 5.5 6 Pack): 978-1-57681-249-5
Note: GOAL/QPC makes no claim to the original US FDA works that may be contained within this book. While the contents of this book are up to date with the April 1st, 2021, edition from the U.S Government, the CFRs are continually revised and as such they may differ from what is contained in this printed book.
21 CFR Part 820, medical device quality and safety
What is FDA's 21 CFR Part 820?
FDA 21 CFR Part 11 Compliance Requirements and Benefits
FDA 21 CFR Part 820 Software
21 CFR Part 820, medical device quality and safety
An overview of 21 CFR Part 820
FDA 21 CFR Part 11 Compliance Checklist
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