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Professional Training
4.4 (21 Reviews)

Clinical Trial Regulatory Requirements

Length
2 days
Price
1,299 GBP 1,099 GBP
Next course start
20 January, 2025 (+3 start dates)
Course delivery
Virtual Classroom
Length
2 days
Price
1,299 GBP 1,099 GBP
Next course start
20 January, 2025 (+3 start dates)
Course delivery
Virtual Classroom
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Clinical Trial Regulatory Requirements

Are you up to date with the regulatory requirements for clinical research in the EU and key requirements in the US?

Do you understand the impact of the new requirements of the EU Clinical Trials Regulation?

This course will take you through the key regulatory and guideline requirements for clinical research in Europe, including the EU Clinical Trial Regulation, ICH GCP R3 update, a brief review of key FDA requirements and update of other recent changes.

This interactive programme will highlight the most important of these key requirements and changes and how these are likely to impact on trials now and in the future for pharmaceutical and biotechnology companies and study sites.

Key topics to be covered include:

  • The EU Clinical trials Regulation (536/2014) and update
  • The New Clinical Trial Information System (CIS)
  • Clinical trial authorisation
  • Complexities for running paediatric trials
  • Requirements for managing investigational medicinal products
  • Legal aspects of clinical trials
  • Requirements for pharmacovigilance
  • ICH GCP R3 update
  • Regulatory inspections

Upcoming start dates

Choose between 3 start dates

20 January, 2025

  • Virtual Classroom
  • Online
  • English

8 May, 2025

  • Virtual Classroom
  • Online
  • English

15 September, 2025

  • Virtual Classroom
  • Online
  • English

Suitability - Who should attend?

Benefits of attending


  • Decipher the framework of clinical trial regulations and guidelines in Europe
  • Gain an update on the new EU Clinical Trial Regulation 536/2014
  • Review key FDA requirements
  • Understand clinical trial authorisations
  • Assess the most important legal aspects of clinical trials
  • Ensure you comply with pharmacovigilance and adverse event reporting

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Reviews by course attendees

Average rating 4.4

Based on 21 reviews.
Reviews are published according to our review policy.
Write a review!
Angela T
5/5
25 May 2023

Excellent and again would only receive this expected type of learning and understanding with the course by IPI Academy. I know that I will have a comprehensive understanding to ...

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Virginie G
4/5
25 May 2023

very interesting
a lot of information and sometimes very fast - so very good to have the material available

Ibrahim B
5/5
14 Jul 2022

Content: Fantastic content and material that would help organisations to prepare for the transition into the CTR

Presentation: Well presented information especially with the in...

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International Professional & Industry Academy
10-12 Rivington Street
EC2A 3DU London

About IPI Academy

International Professional & Industry Academy (IPI) is an international leading professional training organisation based in London. Our training solutions provide a return on your investment with measurable results, and are delivered by experienced professionals and managed with exceptional care and...

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