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Zdrowie i gospodarka · 30.08.2000

Draft Guidance for Industry on Analytical Procedures and Methods Validation: Chemistry, Manufacturing, and Controls Documentation; Availability

The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry entitled "Analytical Procedures and Methods Validation: Chemistry, Manufacturing, and Controls Documentation." This draft guidance is intended to provide recommendations to applicants on submitting analytical procedures, validation data, and samples to support the identity, strength, quality, purity, and potency of drug substances and drug products. The recommendations apply to drug substances and drug products covered in new drug applications (NDA's), abbreviated new drug applications (ANDA's), biologics license applications (BLA's), product license applications (PLA's), and supplements to these applications.

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