Dokumenty (168)
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Kick-off meeting report - ACT EU multi-stakeholder platform
The summary report of the first ACT EU MSP workshop held in June 2023, to understand different stakeholder perspectives on how to transform the EU environment for clinical trials, discuss the feedback from the MSP public consultation and agree on a model for the establishment of the MSP.
Report to monitor the European clinical trials environment (1-30 June 2023, edition 15)
Report to monitor the European clinical trials environment (1-31 May 2023, edition 14)
Report to monitor the European clinical trials environment (1-30 April 2023, edition 13)
Report to monitor the European clinical trials environment (1-31 March 2023, edition 12)
Report to monitor the European clinical trials environment (1-28 February 2023, edition 11)
Report to monitor the European clinical trials environment (1-31 January 2023, edition 10)
Report to monitor the European clinical trials environment (1-31 December 2022, edition 9)
Report to monitor the European clinical trials environment (1-30 November 2022, edition 8)
Report to monitor the European clinical trials environment (1-31 October 2022, edition 7)
Report to monitor the European clinical trials environment (1-30 September 2022, edition 6)
Report to monitor the European clinical trials environment (1-31 August 2022, edition 5)
Report to monitor the European clinical trials environment (1-31 July 2022, edition 4)
Report to monitor the European clinical trials environment (1-30 June 2022, edition 3)
Report to monitor the European clinical trials environment (1-31 May 2022, edition 2)
Report to monitor the European clinical trials environment (31 January – 30 April 2022, edition 1)
Complex clinical trials – questions and answers
Hlavné témy
Recommendation paper on decentralised elements in clinical trials
Annex I - Guidance document on how to approach the protection of personal data and commercially confidential information while using the Clinical Trials Information System (CTIS) Version 2.2
Guidance document on how to approach the protection of personal data and commercially confidential information while using the Clinical Trials Information System (CTIS) Version 2.2
