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This page provides a simple browsing interface for finding entities described by a property and a named value. Other available search interfaces include the page property search, and the ask query builder.

List of results

• Document:DEU SGB V - Sozialgesetzbuch Fünftes Buch 20-Dez-1988  + (DEU SGB V - Sozialgesetzbuch Fünftes Buch 20-Dez-1988)
• Document:DEU StrlSchG - Strahlenschutzgesetz 03-Jan-2022  + (DEU StrlSchG - Strahlenschutzgesetz 03-Jan-2022)
• Document:DEU StrlSchV - Strahlenschutzverordnung 08-Oct-2021  + (DEU StrlSchV - Strahlenschutzverordnung 08-Oct-2021)
• Document:DEU TAMG - Tierarzneimittelgesetz 14-Mar-2024  + (DEU TAMG - Tierarzneimittelgesetz 14-Mar-2024)
• Document:EU 2011/C 172/01 - CT-3 11-Jun-2011  + (EU 2011/C 172/01 - CT-3 11-Jun-2011)
• Document:EU CHMP Guidelines -  + (EU CHMP Guidelines -)
• Document:EU COMMISSION IMPLEMENTING DECISION (EU) 2022/729 11-May-2022  + (EU COMMISSION IMPLEMENTING DECISION (EU) 2022/729 11-May-2022)
• Document:EU Directive 2001/83/EC - Community code relating to medicinal products for human use 20-Jun-12  + (EU Directive 2001/83/EC - Community code relating to medicinal products for human use 20-Jun-12)

• Document:EU EMA Guidelines -  + (EU EMA Guidelines -)

• Document:EU EMA/298712/2022 - Complex clinical trials – Questions and answers 23-May-2022  + (EU EMA/298712/2022 - Complex clinical trials – Questions and answers 23-May-2022)
• Document:EU EMA/431265/2016 Annex I – to guidance for the conduct of good clinical practice inspections – investigator site 06-Sep-2017  + (EU EMA/431265/2016 Annex I – to guidance for the conduct of good clinical practice inspections – investigator site 06-Sep-2017)
• Document:EU EMA/698382/2021 - Guideline for the notification of serious breaches of Regulation (EU) No 536/2014 or the clinical trial protocol 2021  + (EU EMA/698382/2021 - Guideline for the notification of serious breaches of Regulation (EU) No 536/2014 or the clinical trial protocol 2021)
• Document:EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022  + (EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022)
• Document:EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023  + (EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023)
• Document:EU EMA/INS/GCP/126568/2023 - Annual Report of the Good Clinical Practice (GCP) Inspectors' Working Group (IWG) 2022 2023  + (EU EMA/INS/GCP/126568/2023 - Annual Report of the Good Clinical Practice (GCP) Inspectors' Working Group (IWG) 2022 2023)
• Document:EU EMA/INS/GCP/143492/2022 - ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE 2022  + (EU EMA/INS/GCP/143492/2022 - ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE 2022)
• Document:EU EMA/INS/GCP/856758/ 2018 Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic) 06-Dec-2018  + (EU EMA/INS/GCP/856758/ 2018 Guideline on the content, management and archiving of the clinical trial master file (paper and/or electronic) 06-Dec-2018)
• Document:EU EMEA/CHMP/313666/2005 - GUIDELINE ON THE EXPOSURE TO MEDICINAL PRODUCTS DURING PREGNANCY: NEED FOR POST-AUTHORISATION DATA 14-Nov-2005  + (EU EMEA/CHMP/313666/2005 - GUIDELINE ON THE EXPOSURE TO MEDICINAL PRODUCTS DURING PREGNANCY: NEED FOR POST-AUTHORISATION DATA 14-Nov-2005)
• Document:EU ENCePP - Guide on Methodological Standards in Pharmacoepidemiology Revision 11 (2023)  + (EU ENCePP - Guide on Methodological Standards in Pharmacoepidemiology Revision 11 (2023))
• Document:EU EudraLex – Volume 10 -  + (EU EudraLex – Volume 10 -)
• Document:EU Eudralex - volume 4 GMP Guidelines Annex 11 Jan-2011  + (EU Eudralex - volume 4 GMP Guidelines Annex 11 Jan-2011)
• Document:EU Eudralex - volume 4 GMP Guidelines Chapter 4 Jan-2011  + (EU Eudralex - volume 4 GMP Guidelines Chapter 4 Jan-2011)
• Document:EU European Medicines Agency’s Data Protection: Notice For Microsoft (MS) Copilot 365 - EMA pilot phase ; EMA/216030/2025 45838  + (EU European Medicines Agency’s Data Protection: Notice For Microsoft (MS) Copilot 365 - EMA pilot phase ; EMA/216030/2025 45838)
• Document:EU GUIDANCE ON THE MANAGEMENT OF CLINICAL TRIALS DURING THE COVID-19 (CORONAVIRUS) PANDEMIC v5 10-Feb-2022  + (EU GUIDANCE ON THE MANAGEMENT OF CLINICAL TRIALS DURING THE COVID-19 (CORONAVIRUS) PANDEMIC v5 10-Feb-2022)
• Document:EU GVP: Module VIII EMA/813938/2011 Rev. 3 (2017)  + (EU GVP: Module VIII EMA/813938/2011 Rev. 3 (2017))
• Document:EU GVP: Module XVI EMA/204715/2012 Rev. 3 (2024)  + (EU GVP: Module XVI EMA/204715/2012 Rev. 3 (2024))
• Document:EU INS/GCP/46309/2012 - Classification and analysis of the GCP inspection findings of GCP inspections conducted at the request of the CHMP 2012  + (EU INS/GCP/46309/2012 - Classification and analysis of the GCP inspection findings of GCP inspections conducted at the request of the CHMP 2012)
• Document:EU MDCG Guidelines -  + (EU MDCG Guidelines -)
• Document:EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017  + (EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017)
• Document:EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22  + (EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22)
• Document:EU Regulation (EU) 2016/679 (GDPR) 04-May-2016  + (EU Regulation (EU) 2016/679 (GDPR) 04-May-2016)
• Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble  + (EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble)
• Document:EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023  + (EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023)
• Document:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023  + (EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023)