Research and Markets, the largest resource for market research information in world providing essential market research reports, industry research, industry analysis, forecasts, market studies, company profiles and country reports.
Welcome - Register - Login - Help/FAQ - 0 items View Basket
Worlds Largest Market Research Resource - 1516232 Live Reports
Search Research and Markets
  Search
Enter keywords, a title or
a report id number below.





Advanced   
Company search
Register for free email updates of market research
Currency
  Select a currency for use throughout the site



Viewing report

Order by Fax
Ask a Question
Printer Friendly
PDF Brochure
Hard CopyAdd to Basket
Live Chat Live Help Software for Website

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

Informa Healthcare, Dec 2004, Pages: 452


  Description  
   Table of Contents   
   Author   
    
    
     
  Enquire before Buying   
  Send to a Friend   

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.



Customers who bought this item also bought

GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers, Sixth Edition, (Volume 1 - With Checklists and Software Package)

GMP/ISO/EN Quality Audit Manual for Healthcare Manufacturers and Their Suppliers, Fifth Edition, (Volume I - Checklists)

GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers, Sixth Edition (2 Volume Set)

Pharmaceutical Computer Systems Validation: Quality Assurance, Risk Management and Regulatory Compliance, Second Edition

Cost-Contained Regulatory Compliance: For the Pharmaceutical, Biologics, and Medical Device Industries

Handbook of Pharmaceutical Manufacturing Formulations, Second Edition: (Six-Volume Set)

2011 CFR/ICH GCP Reference Guide for Medical Devices

Medical Devices Manual

2011 Code of Federal Regulations Reference Guide for Medical Devices

Handbook of Pharmaceutical Manufacturing Formulations



For enquiries please call us on:
  +353-1-415-1241 (GMT Office Hours)
  1-800-526-8630 (US/Canada Toll Free)
  1-917-300-0470 (EST Office Hours)

   All rights reserved. © Copyright 2012 Research and Markets
   Terms and conditions Privacy Policy Publishers Employment Opportunities Site Map Link to us Webmaster Affiliate Network


Research and Markets RSS Feeds