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Accelerating Clinical Trials in the EU

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  • General publications
  • 5 November 2024
Meeting highlights - MSP Advisory Group 27 September 2024
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  • General publications
  • 4 November 2024
MSP Advisory Group Mandate and rules of procedure
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  • General publications
  • 18 October 2024
Short, medium, long term actions proposed by Industry trade associations
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  • General publications
  • 17 October 2024
New CTIS Public Portal functionality
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  • General publications
  • 17 October 2024
Approach to consulting academic stakeholders
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  • General publications
  • 17 October 2024
Discussion on stakeholder priorities to advise ACT EU Steering Group
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  • General publications
  • 17 October 2024
Report from CTR Collaborate stakeholder meeting held on 11 September
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  • General publications
  • 17 October 2024
MSP AG report on the most frequently reported and major issues
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  • General publications
  • 15 October 2024
Key performance indicators (KPIs) to monitor the European clinical trials environment (1-30 September 2024)
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  • General publications
  • 8 October 2024
Member States participating in ACT EU pilots on consolidated advice
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  • General publications
  • 23 September 2024
Agenda MSP Advisory Group meeting 27 September 2024
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  • General publications
  • 20 September 2024
Meeting highlights - MSP Advisory Group 4 July 2024
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  • General publications
  • 17 September 2024
Key performance indicators (KPIs) to monitor the European clinical trials environment (1-31 August 2024)
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  • General publications
  • 12 August 2024
Key performance indicators (KPIs) to monitor the European clinical trials environment (1-31 July 2024)
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  • General publications
  • 25 July 2024
Key performance indicators (KPIs) to monitor the European clinical trials environment (1-30 June 2024)
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  • General publications
  • 8 July 2024
Challenges and possible options when designing a Platform Trial - F. Houyez (EURORDIS)

Challenges and possible options when designing a Platform Trial -  F. Houyez (EURORDIS)

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  • General publications
  • 8 July 2024
Challenges in performing mult-country Investigator Initiated Trials in EU - M. Zuidgeest (UMC Utrecht)

Challenges in performing mult-country Investigator Initiated Trials in EU - M. Zuidgeest (UMC Utrecht)

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  • General publications
  • 8 July 2024
CTA review process and CTR implementation - L. Leyens (EFPIA)

CTA review process and CTR implementation - L. Leyens (EFPIA)

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  • General publications
  • 8 July 2024
Enabling CTIS Public Data Use - F. Sweeney (CDDF)

Enabling CTIS Public Data Use - F. Sweeney (CDDF)

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  • General publications
  • 8 July 2024
Enhancing and harmonizing Regulatory process for clinical trials- M. Heath (Vaccines Europe)

Enhancing and harmonizing Regulatory process for clinical trials- M. Heath (Vaccines Europe)