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NOTE FOR GUIDANCE ON GOOD CLINICAL PRACTICE Historical document These guidelines may be overridden by national legal requirements and the requirements of

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The list below contains all the Guidance Documents which are available, or will be available, on this website. Guidance on requirements for substances in articles .

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Cultural heritage policies are included in the third chapter of this document. (HPAC), Municipal Heritage Design Guidelines. It provides additional guidance

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FDA Guidance for Industry Update – Process Validation guidance document, Guideline on General Principles of FDA Guidance for Industry Update – Process

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Guidance document which relates to FDA 21 CFR 820.30 and Sub-clause 4.4 of ISO Guidelines Detail; FDA DESIGN CONTROL GUIDANCE FOR MEDICAL DEVICE MANUFACTURERS.

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Clinical evidence guidelines documents for medical devices. 28 February 2017. This document is intended to provide guidance to manufacturers of medical devices

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