QualityIn-QualityOut-Webinar_340x230Quality In, Quality Out: Regulatory Drivers of Supplier Quality Management in the Medical Device Industry

The third in a four-part series, this webinar takes a look at 21 CFR Part 11, as well as various drug guidelines, providing direction and industry views on how the FDA interprets purchasing controls for drug manufacturers and their suppliers.

Topics addressed in this presentation include:

  • International regulations and their correlation to FDA requirements as they relate to drug manufacturing quality systems
  • The most common FDA enforcement actions (483 Observations, Warning Letters)
  • Recent FDA statistics on the increasing number of drug product recalls

Watch this on-demand webinar to learn more. »