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

Compliance Auditing for Pharmaceutical Manufacturers: A Practical Guide to In-Depth Systems Auditing

Informa Healthcare, Aug 1994, Pages: 408


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

Focusing on the practical aspects of GMP auditing, Compliance Auditing for Pharmaceutical Manufacturers provides a hands-on approach for performing audits - what questions to ask and what answers to expect - that will save QA professionals and department heads alike time and effort while ensuring compliance. The amount of verbiage has deliberately been kept to a minimum. The purpose of any prose is to supplement the checklists by explaining how to use them and how to determine whether responses are satisfactory. After reading this manual, readers will be able to enter any department in their company or in any other company and perform an in-depth, effective, and efficient cGMP compliance audit.

Features



Customers who bought this item also bought

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

Handbook of Pharmaceutical Manufacturing Formulations

Dietary Supplement Good Manufacturing Practices: Preparing for Compliance

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

Japan Quality Audits 2010

Pre-Clinical Stage Partnering Terms and Agreements in Pharma, Biotech and Diagnostics, 2nd Edition

Handbook of Pharmaceutical Manufacturing Formulations Series, Second Edition, Volume 5: Over-the-Counter Products

Handbook of Pharmaceutical Manufacturing Formulations Series: Over-the-Counter Products

Handbook of Pharmaceutical Manufacturing Formulations: Over-the-Counter Products

Quality Assurance for Medical Devices in China



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