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Property:DocRestricted

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Text

Whether access is restricted (Yes/No).

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Showing 20 pages using this property.
D
DEU SGB V - Sozialgesetzbuch Fünftes Buch 20-Dez-1988 +
No  +
DEU StrlSchG - Strahlenschutzgesetz 03-Jan-2022 +
No  +
DEU StrlSchV - Strahlenschutzverordnung 08-Oct-2021 +
No  +
DEU TAMG - Tierarzneimittelgesetz 14-Mar-2024 +
No  +
E
EU 2011/C 172/01 - CT-3 11-Jun-2011 +
No  +
EU CHMP Guidelines - +
No  +
EU COMMISSION IMPLEMENTING DECISION (EU) 2022/729 11-May-2022 +
No  +
EU Directive 2001/83/EC - Community code relating to medicinal products for human use 20-Jun-12 +
No  +
EU EMA Guidelines - +
No  +
EU EMA/298712/2022 - Complex clinical trials – Questions and answers 23-May-2022 +
No  +
EU EMA/431265/2016 Annex I – to guidance for the conduct of good clinical practice inspections – investigator site 06-Sep-2017 +
No  +
EU EMA/698382/2021 - Guideline for the notification of serious breaches of Regulation (EU) No 536/2014 or the clinical trial protocol 2021 +
No  +
EU EMA/786433/2022 Annex V – to guidance for the conduct of good clinical practice inspections – Phase I units 15-Nov-2022 +
No  +
EU EMA/INS/GCP/112288/2023 - Guideline on computerised systems and electronic data in clinical trials 2023 +
No  +
EU EMA/INS/GCP/126568/2023 - Annual Report of the Good Clinical Practice (GCP) Inspectors' Working Group (IWG) 2022 2023 +
No  +
EU EMA/INS/GCP/143492/2022 - ANNEX I TO PROCEDURE FOR CONDUCTING GCP INSPECTIONS REQUESTED BY THE CHMP: INVESTIGATOR SITE 2022 +
No  +
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 +
No  +
EU EMEA/CHMP/313666/2005 - GUIDELINE ON THE EXPOSURE TO MEDICINAL PRODUCTS DURING PREGNANCY: NEED FOR POST-AUTHORISATION DATA 14-Nov-2005 +
No  +
EU ENCePP - Guide on Methodological Standards in Pharmacoepidemiology Revision 11 (2023) +
No  +
EU EudraLex – Volume 10 - +
No  +
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