The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) prepares scientific guidelines in consultation with regulatory authorities in the European Union (EU) Member States, to help applicants prepare marketing-authorisation applications for human medicines. Guidelines provide a basis for practical harmonisation of how the EU Member States and the Agency interpret and apply the detailed requirements for the demonstration of quality, safety and efficacy that are in the Community directives.
Related Journals of Europian regulatory guidelines
Clinical Research and Regulatory Affairs, Generics and biosimilars initiative Journal
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Jan 01, 1970
Accepted Date: Jan 01, 1970
Published Date: Jan 01, 1970