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Property:DocLanguage

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ISO 639 language code(s) of the document.

previous 202050100250500next 20
Showing 20 pages using this property.
E
EU ENCePP - Guide on Methodological Standards in Pharmacoepidemiology Revision 11 (2023) +
EN  +
EU EudraLex – Volume 10 - +
EN  +
EU Eudralex - volume 4 GMP Guidelines Annex 11 Jan-2011 +
EN  +
EU Eudralex - volume 4 GMP Guidelines Chapter 4 Jan-2011 +
EN  +
EU GUIDANCE ON THE MANAGEMENT OF CLINICAL TRIALS DURING THE COVID-19 (CORONAVIRUS) PANDEMIC v5 10-Feb-2022 +
EN  +
EU GVP: Module VIII EMA/813938/2011 Rev. 3 (2017) +
EN  +
EU GVP: Module XVI EMA/204715/2012 Rev. 3 (2024) +
EN  +
EU INS/GCP/46309/2012 - Classification and analysis of the GCP inspection findings of GCP inspections conducted at the request of the CHMP 2012 +
EN  +
EU MDCG Guidelines - +
EN  +
EU Recommendations of the expert group - Risk proportionate approaches in clinical trials 25-Apr-2017 +
EN  +
EU Regulation (EC) No 726/2004 - authorisation and supervision of medicinal products for human use 28-Jan-22 +
EN  +
EU Regulation (EU) 2016/679 (GDPR) 04-May-2016 +
EN  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 05-May-2017 Preamble +
EN  +
EU Regulation (EU) 2017/745 - Medical Device Regulation 20-Mar-2023 +
EN  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 05-May-2017 Preamble +
EN  +
EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 +
EN  +
EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 +
EN  +
EU Regulation (EU) 536/2014 - clinical trials 27-May-2014 Preamble +
EN  +
EU Regulation (EU) 910/2014 - electronic identification 17-Sep-2014 +
EN  +
EU Regulation (EU) No 520/2012 - performance of pharmacovigilance activities 20-Jun-12 +
EN  +
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