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Documents (157)
RSSQed jintwerew ir-riżultati 120 sa 140
Report to monitor the European clinical trials environment (1-31 January 2024)
Report to monitor the European clinical trials environment (1-31 December 2023)
Report to monitor the European clinical trials environment (1-30 November 2023)
Revised CTIS transparency rules & historical trials: quick guide for users
ACT EU priority areas for possible EU-level funding
Report to monitor the European clinical trials environment (1-31 October 2023)
Enfasizzat
ACT EU multi-annual workplan 2023-2026
Report to monitor the European clinical trials environment (1-30 September 2023)
Report to monitor the European clinical trials environment (1-31 August 2023)
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)
