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Property:RefModule

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Module number this reference belongs to.

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Showing 20 pages using this property.
W
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - sponsor +
2  +
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - contract research organization (CRO) +
2  +
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.17 +
2  +
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 5 +
2  +
I
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 9 +
2  +
E
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Annex XV Chapter III 2. ; 7. +
2  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Annex XIV Chapter II Section 2 +
2  +
D
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 4 Absatz 24 +
2  +
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 40b-002 +
2  +
G
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 3 (1) - (5) +
2  +
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 3 (6) - (11) +
2  +
U
USA 21 CFR Part 50 09-Apr-2025 § 50.3 (e) +
2  +
USA 21 CFR Part 50 09-Apr-2025 § 50.3 (f) +
2  +
USA 21 CFR Part 312 09-Apr-2025 § 312.3 (b) - Sponsor +
2  +
USA 21 CFR Part 312 09-Apr-2025 § 312.3 (b) - Sponsor-Investigator +
2  +
USA 21 CFR Part 312 09-Apr-2025 § 312.3 (b) - CRO +
2  +
USA 21 CFR Part 312 09-Apr-2025 § 312.50 +
2  +
USA 21 CFR Part 312 09-Apr-2025 § 312.52 +
2  +
USA 21 CFR Part 312 09-Apr-2025 § 312.53 +
2  +
USA 21 CFR Part 54 09-Apr-2025 § 54.4 list of investigators +
2  +
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