Personal tools

Sponsorname

Your company could advertise here

www.fla-consulting.eu

Glossary:TAG-00044-Ins-ion

From GxPlex

Revision as of 17:29, 15 July 2026 by gxplex>GxPlexBot (Import from GxPlex Excel)
Jump to: navigation, search


Glossary > Inspection

Inspection
Tag-ID TAG-00044-Ins-ion
English Inspection / GCP inspection / Regulatory inspection
French Inspection / Inspection des bonnes pratiques cliniques / Inspection réglementaire
German Inspektion / GCP-Inspektion / Behördliche Inspektion

References

 ScopeDocument partLanguageDocument
AUT BASG - FAQ 11-Feb-2025 SchwarzGSchwarzDEAUT BASG - FAQ 11-Feb-2025
DEU AMG - Arzneimittelgesetz 19-Jul-2023 § 42cHM§ 42cDEDEU AMG - Arzneimittelgesetz 19-Jul-2023
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 68MD§ 68DEDEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 77MD§ 77DEDEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022
DEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022 § 79MD§ 79DEDEU MPDG - Medizinprodukterecht-Durchführungsgesetz 28-Jun-2022
EU EMA/INS/GCP/126568/2023 - Annual Report of the Good Clinical Practice (GCP) Inspectors' Working Group (IWG) 2022 2023 4.3G4.3ENEU EMA/INS/GCP/126568/2023 - Annual Report of the Good Clinical Practice (GCP) Inspectors' Working Group (IWG) 2022 2023
EU INS/GCP/46309/2012 - Classification and analysis of the GCP inspection findings of GCP inspections conducted at the request of the CHMP 2012 5G5ENEU INS/GCP/46309/2012 - Classification and analysis of the GCP inspection findings of GCP inspections conducted at the request of the CHMP 2012
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 ANNEX XV Chapter III, 6MDANNEX XV Chapter III, 6ENEU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 Article 72 Pragraph 5MDArticle 72 Pragraph 5ENEU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 68 Paragraph 5IVDArticle 68 Paragraph 5ENEU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 78HMArticle 78ENEU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022
GBR Directive 2001/20/EC 04-Apr-2001 Article 2 (l)HMArticle 2 (l)ENGBR Directive 2001/20/EC 04-Apr-2001
GBR Guidance - Good clinical practice for clinical trials 16-Oct-2015 -HM-ENGBR Guidance - Good clinical practice for clinical trials 16-Oct-2015
GBR MHRA GCP Inspection Dossier template V7.0 -G-ENGBR MHRA GCP Inspection Dossier template V7.0
ICH ICH E6 Guideline R3 (2025) GLOSSARY - InspectionGGLOSSARY - InspectionENICH ICH E6 Guideline R3 (2025)
ICH ICH E6 Guideline R3 (2025) GLOSSARY - Regulatory AuthoritiesGGLOSSARY - Regulatory AuthoritiesENICH ICH E6 Guideline R3 (2025)
ISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020 7.11MD7.11ENISO ISO 14155 - Clinical investigation of medical devices for human subjects 2020
USA 21 CFR Part 312 09-Apr-2025 § 312.58HM§ 312.58ENUSA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 312 09-Apr-2025 § 312.68HM§ 312.68ENUSA 21 CFR Part 312 09-Apr-2025
USA 21 CFR Part 812 09-Apr-2025 § 812.145MD§ 812.145ENUSA 21 CFR Part 812 09-Apr-2025
USA FDA Information - Observations and citations 20-Mar-2024 -G-ENUSA FDA Information - Observations and citations 20-Mar-2024
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 11.2HM11.2ENWHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.12-002HM4.12ENWHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 4.12-003HM4.12ENWHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995
WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - inspectionHMGlossary - inspectionENWHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995