Join Amazon Prime and ship Two-Day for free and Overnight for $3.99. Already a member? Sign in.
GMP/ISO Quality Audit Manual for Healthcare Manufacturers... and over 190,000 other books are available for Amazon Kindle – Amazon’s new wireless reading device. Learn more

 

or
Sign in to turn on 1-Click ordering.
 
   
More Buying Choices
11 used & new from $295.00

Have one to sell? Sell yours here
 
   
GMP/ISO Quality Audit Manual for Healthcare Manufacturers and their Suppliers, Sixth Edition, (Volume 1 -  With Checklis
 
 
Start reading GMP/ISO Quality Audit Manual for Healthcare Manufacturers... on your Kindle in under a minute.

Don’t have a Kindle? Get yours here.
 
  

GMP/ISO Quality Audit Manual for Healthcare Manufacturers and their Suppliers, Sixth Edition, (Volume 1 - With Checklis (Ring-bound)

by Leonard Steinborn (Author)
Key Phrases: organization analyze appropriate data, quality audit manual, retrieval mechanism exist, United States, Documentation Controls, Rating Reference (more...)
No customer reviews yet. Be the first.

List Price: $399.95
Price: $356.49 & this item ships for FREE with Super Saver Shipping. Details
You Save: $43.46 (11%)
In Stock.
Ships from and sold by Amazon.com. Gift-wrap available.

Only 1 left in stock--order soon (more on the way).

Want it delivered Wednesday, December 3? Choose One-Day Shipping at checkout. See details

Ordering for Christmas? To ensure delivery by December 24, choose FREE Super Saver Shipping at checkout. Read more about holiday shipping.

8 new from $295.00 3 used from $488.41
Also Available in: List Price: Our Price: Other Offers:
Kindle Edition (Kindle Book) $159.96
Hardcover (6) $649.95 $649.95 7 used & new from $645.11
Paperback (1) $329.95 $286.02 9 used & new from $189.33
 
   

Editorial Reviews

Product Description
Volume 1 of this two-part package provides a complete set of checklists for internal and contract device and drug manufacturers and developers, contract software developers, and suppliers of chemical, printed material, electronic component, and general supplies. It also includes a simulated QSIT audit, and a new-product market launch. All of these are referenced to the relevant relevant FDA regulations, EC and IPEC guidelines, and ISO/BSI standards. The text also explains various audit types, do's and don'ts for auditors, and guidance for audit preparation, performance, conclusion, report derivation, and follow up activities. A CD-ROM packaged with the book contains all of the checklists in a customizable electronic format.