Learn what are the best practices for correcting GMP documentation errors, based on the FDA and other regulatory guidelines, and why, how, when, who and what to do after correcting them.

During this 1-hour webinar, we will review the Good Documentation Practices plus demonstrate examples of these practices (both good and bad!) as they apply to the pharmaceutical arena. Why you should ...

Where things go wrong most often where more than one system is in operation is with documentation. GMP requires not only good documentation practice, but also must meet the strict requirements for ...