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5.0 (1 Reviews)

Risk Management for Clinical Research

Length
1 day
Price
649 GBP 549 GBP
Next course start
4 February, 2025 (+3 start dates)
Course delivery
Virtual Classroom
Length
1 day
Price
649 GBP 549 GBP
Next course start
4 February, 2025 (+3 start dates)
Course delivery
Virtual Classroom
Visit this course's homepage on the provider's site to learn more or book!

Risk Management for Clinical Research

Risk management is becoming increasingly important in clinical trials, as well as in ensuring compliance with regulatory expectations. Numerous pharmaceutical guidelines now cover risk management in clinical trials, including ICH GCP R2 and R3, and the FDA's Risk-Based Monitoring of Clinical Investigations: Questions and Answers guidance.

During this one-day course you will learn how to apply a risk-based approach when managing your clinical trials lifecycle. We will review the principles of risk management and how to apply them within a clinical trial setting according to ICH GCP R2 and R3.

This essential course will explain the importance of using risk management techniques in clinical development to comply with the latest focus on inspection in this area. It will show you how risk management can improve the quality of your clinical research projects and demonstrate the importance of using risk analysis and risk management techniques in clinical trials. You will learn how to identify, evaluate and implement specific risk-based techniques for risk management, including a quality management framework.

The course will enable you to develop quality risk management principles applicable to clinical trials, pharma, biopharma and device development, as well as to identify and share best practices for risk management tools and approaches.

Upcoming start dates

Choose between 3 start dates

4 February, 2025

  • Virtual Classroom
  • Online
  • English

6 June, 2025

  • Virtual Classroom
  • Online
  • English

7 October, 2025

  • Virtual Classroom
  • Online
  • English

Suitability - Who should attend?

Benefits of attending

  • Understand risk management tools and when and how the tools are used in pharmaceutical, biopharmaceutical and medical device projects
  • Learn how to plan risk-based approaches, how to document and where to focus to meet regulatory requirements and expectations
  • Develop and apply risk management principles and tools to your development projects
  • Identify and share best practices for implementing risk-based tools and principles
  • Gain a clear understanding of the objectives outlined in ICH Guidance E6 and E8 concerning risk management in clinical trials

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Reviews by course attendees

Average rating 5

Based on 1 reviews.
Reviews are published according to our review policy.
Write a review!
Arna Hrund A
5/5
14 Oct 2022

Very good

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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