Property:RefLanguage
From GxPlex
Language of this reference.
E
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G
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USA FDA - E6(R2) Good Clinical Practice: Integrated Addendum to ICH E6(R1): Guidance for Industry March 2018 - +
EN +
USA Acceptance of Clinical Data to Support Medical Device Applications and Submissions Frequently Asked Questions - Guidance for Industry and Food and Drug Administration Staff 21-Feb-2018 - +
EN +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - 1.5 Regulatory requirements +
EN +
I
W
U
I
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Institutional Review Board (IRB)/Independent Ethics Committee (IEC) +
EN +
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - ethics committee +
EN +
I
