SALT LAKE CITY UT USA - Nov. 6, 2006 - The FDA recently issued a final guidance meant to help pharmaceutical companies operate modern quality systems that are fully compliant with Current Good Manufacturing Practice (CGMP) regulations.
Download the Q&A:
www.mastercontrol.com/land/email/quality_systems_approach_pharmaceutical_cgmp.php5?AID=imail-pharma-cgmp This question-and-answer article prepared by MasterControl provides pertinent facts about the FDA's "Guidance on Quality Systems Approach to Pharmaceutical CGMP Regulations," issued on Sept. 29, 2006.
The Q&A covers the following:
- What this guidance means in a nutshell and who is covered by it.
- Six-System Inspection Model.
- Quality Systems Model.
- How MasterControl can help manufacturers attain a CGMP-compliant quality system.
About MasterControl
MasterControl Inc. has been at the forefront of providing innovative quality management software solutions since 1993.
Over 400 companies worldwide use the MasterControl solution to consistently meet FDA regulations, ISO standards, and other regulatory requirements.
In addition to providing off-the-shelf products, MasterControl also offers comprehensive technical and customer support, including product training, installation, implementation, and validation services.
