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Zdrowie i gospodarka · 18/08/2003

FDA Releases Draft Guidance for Chemistry, Manufacturing, and Control Reviewers of Human Somatic Cell Therapy INDs

The FDA has made available a draft document outlining instructions and a template for reviewers of human somatic cell therapy Investigational New Drug Applications (INDs) to assess and record relevant information, aiming to finalize the guidance by an unspecified date.

Source: Federal Register — Food and Drug AdministrationOpen original release →