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Glossary:TAG-00018-Inv-die

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Glossary > Investigator

Investigator
Tag-ID TAG-00018-Inv-die
English Investigator / Researcher
EN Abbr. I
French Investigateur / Investigatrice / Chercheur / Chercheuse
German Prüfer / Prüferin / Studienarzt / Studienärztin

References

 ScopeDocument partLanguageDocument
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 4 Absatz 25HM§ 4 Absatz 25DEDEU AMG - Arzneimittelgesetz 19-Jul-2023
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 30-001MD§ 30DEDEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 30-002MD§ 30DEDEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022
EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022 2.5-002G2.5ENEU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 58 Paragraph 7 – 8IVDArticle 58 Paragraph 7 – 8ENEU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 49HMArticle 49ENEU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 15 (5) (d)HMArticle 15 (5) (d)ENGBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004
GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 investigatorHMArticle 2 investigatorENGBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004
ICH ICH E6 Guideline R3 (2025) GLOSSARY - InvestigatorGGLOSSARY - InvestigatorENICH ICH E6 Guideline R3 (2025)
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Sponsor-InvestigatorGGLOSSARY - Sponsor-InvestigatorENICH ICH E6 Guideline R3 (2025)
ICH ICH E6 Guideline R3 (2025) III. Annex 1 2GIII. Annex 1 2ENICH ICH E6 Guideline R3 (2025)
USA 21 CFR Part 312 09-Apr-2025 § 312.3 (b) - Sponsor-InvestigatorHM§ 312.3 (b) - Sponsor-InvestigatorENUSA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 312 09-Apr-2025 § 312.3 - InvestigatorHM§ 312.3 - InvestigatorENUSA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 312 09-Apr-2025 § 312.53HM§ 312.53ENUSA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 312 09-Apr-2025 § 312.70HM§ 312.70ENUSA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 50 09-Apr-2025 § 50.3 (d)G§ 50.3 (d)ENUSA 21 CFR Part 50 09-Apr-2025
USA 21 CFR Part 50 09-Apr-2025 § 50.3 (f)G§ 50.3 (f)ENUSA 21 CFR Part 50 09-Apr-2025
USA 21 CFR Part 54 09-Apr-2025 § 54.4 disclosureG§ 54.4 disclosureENUSA 21 CFR Part 54 09-Apr-2025
USA 21 CFR Part 54 09-Apr-2025 § 54.4 list of investigatorsG§ 54.4 list of investigatorsENUSA 21 CFR Part 54 09-Apr-2025
USA 21 CFR Part 56 09-Apr-2025 § 56.109G§ 56.109ENUSA 21 CFR Part 56 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.119MD§ 812.119ENUSA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.3 (i)MD§ 812.3 (i)ENUSA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.3 (o)MD§ 812.3 (o)ENUSA 21 CFR Part 812 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.43MD§ 812.43ENUSA 21 CFR Part 812 09-Apr-2025
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 1.4HM1.4ENWHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.17HM4.17ENWHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.2HM4.2ENWHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - investigatorHMGlossary - investigatorENWHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - sponsorHMGlossary - sponsorENWHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
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