UNLIMITED FREE
ACCESS
TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your GlobalSpec Experience

Finish!
Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

CRC - TFE325

GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers, (Volume 2 - Regulations, Standards, and Guidelines) : Regulations, Standards, and Guidelines

active, Most Current
Organization: CRC
Publication Date: 30 December 2004
Status: active
Page Count: 453
scope:

This well-known QA manual has been updated to provide the guidance readers need to assess their compliance with standard regulations. This Volume 2 of a three-part package contains the full text on:
* FDA regulations
* EC and IPEC guidelines
* ISO/BSI standards referenced in the checklists furnished in volume 1
Easy-to-read and organized to provide fast access to guidelines and regulations, this is an essential reference for those working in the field.

Document History

TFE325
December 30, 2004
GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers, (Volume 2 - Regulations, Standards, and Guidelines) : Regulations, Standards, and Guidelines
This well-known QA manual has been updated to provide the guidance readers need to assess their compliance with standard regulations. This Volume 2 of a three-part package contains the full text on:...
Advertisement