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PIC/S Sets Roadmap on GMP Projects for Next Two Years

March 15, 2017

A group of drug regulators is considering boosting resources for training inspectors, improving international cooperation, and revising guidelines on sterile manufacturing over the next two years.

The Pharmaceutical Inspection Co-operation Scheme — which comprises dozens of regulatory authorities, including the FDA — set a roadmap for its GMP harmonization projects, saying the group intends to work on further implementing its training program and improving collaborations with other associations, such as the International Coalition of Medicines Regulatory Authorities.

Other priorities outlined in the roadmap include strengthening the group’s position on advanced therapy medicinal products (ATMPs) and revising GMP guidelines.

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