Thursday 18 April 2013


One of the top discussion blogs available on the Internet is the "WHO cGMP" blog. The site features most of the latest standards and guidelines, and contains invaluable advice for their implementation.

As the site indicates, it covers:

FDA GMP Guidelines Pharma Validation Pharma Process Validations Clean Room Classification 21 CFR Part 11 compliance Clinical Trials, Sterile Aseptic Process Training Sterile Dosage Form,Good Manufacturing Practices Pharmaceutical Companies Pharmaceutical Industry FDA Guide Pharma Regulatory Affairs In Pharmaceutical SOP'S Requirements of Manufacturing Documentation Quality Assurance SOP'S For Microbiology Department Pharma Manufacturing Firm Questions Answers.

And goes onto explain:

"Are you associated with pharmaceutical validation pharma regulatory affairs pharmaceutical manufacturing pharmaceutical process validation and are looking for quality information about pharmaceutical manufacturing and process validation US FDA guidelines Pharmaceutical Current Good Manufacturing practices GMP Guidelines C gmp practices across the world ?

Are you a pharmacist working in Pharmaceutical Regulatory Affairs in a pharmaceutical company, pharmacy, in pharmaceutical manufacturing, Quality assurance ?"

For more information, see the "WHO GMP" site.

Posted by Tim Sandle

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