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4.5 (21 Reviews)

Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application

Length
2 sessions of
Price
649 GBP 549 GBP
Next course start
23 October, 2024 (+4 start dates)
Course delivery
Virtual Classroom
Length
2 sessions of
Price
649 GBP 549 GBP
Next course start
23 October, 2024 (+4 start dates)
Course delivery
Virtual Classroom
Leave your details so the provider can get in touch

Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application

The Common Technical Document (CTD) Guideline is the obligatory format in the EU and most territories worldwide for registration applications. The clinical overview and clinical summaries in Module 2 provide a critical analysis of the clinical data within the CTD.

This interactive course will present the regulatory guidelines and requirements of Module 2 and discuss practical approaches to developing the content and preparation of the clinical overview and clinical summaries. The programme will provide a review of the latest information and potential future developments and cover associated documents, such as the RMP and SmPC. A practical workshop session will simulate real situations and highlight the key issues to consider when preparing the content of the written summary.

Upcoming start dates

Choose between 4 start dates

23 October, 2024

  • Virtual Classroom
  • Online
  • English

5 February, 2025

  • Virtual Classroom
  • Online
  • English

18 June, 2025

  • Virtual Classroom
  • Online
  • English

1 October, 2025

  • Virtual Classroom
  • Online
  • English

Suitability - Who should attend?

Benefits of attending

  • Gain practical advice on writing clinical documents for global submissions
  • Review the latest guidance to ensure you meet regulatory expectations
  • Understand how to prepare separate integrated summaries of efficacy and safety for FDA
  • Clarify the content of orphan drug applications, over-the-counter (OTC) switches, line extensions and safety-related labelling updates
  • Ensure your risk management plan (RMP) is consistent with the Common Technical Document (CTD)
  • Discuss the place of the clinical overview and summary in life cycle knowledge from initial IB to PSUR, and how they support the changing summary of product characteristics (SmPC)

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Reviews by course attendees

Average rating 4.5

Based on 21 reviews.
Reviews are published according to our review policy.
Write a review!
Marco T
5/5
07 Feb 2024

John Price explained all information in practical and useful way. I have been satisfied from the whole shapes of the program. For sure I will recommend it to other colleagues.

Caroline B
4/5
04 Oct 2023

I wanted to broaden my knowledge of submissions, I think it's accomplished

Angela T
5/5
28 Jun 2023

Very well organized and detail to address areas I would not have considered - very grateful they were addressed! I received more value that I anticipated and would absolutely re...

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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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