EMA-FDA Joint GMP and GCP Inspection Pilot Programs

Posted 01 October 2011 | By Michelle Conan-Cibotti, PhD, RAC 

The global harmonization of regulatory requirements for the registration of pharmaceutical products started in the 1990s with the International Conference on Harmonisation (ICH). Ensuring consistent interpretation and implementation of ICH guidelines and continuous delivery of safe and effective products to consumers remains a challenge for regulators and industries.

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