Clinical Trial Risk Management in Practice

Understand risk management principles and the links between study level risk management and the implementation of risk based monitoring

14. Dec 2021
13. Dec 2022

2 days course

English

8,100 DKK ex VAT
(app. 1,089 EUR ex VAT)
50% DISCOUNT FOR PUBLIC INSTITUTIONS

Summary

In this course you will get the basic tools to apply a risk-based approach when managing your clinical trial. We will review the principles of risk management and how to apply them within a clinical trial setting according to ICH GCP E6(R2).

You will also get the opportunity to practice the necessary skills when we look at examples from actual inspections and discuss how to apply a risk-based approach on areas where change is needed.

Along with identification and evaluation of risks in critical processes, study data and clinical trial operations, it is imperative to ensure that the necessary processes are in place. This course will allow you to appraise your current processes, people and technology with a view to improve oversight and enhance patient protection while maintaining high quality data.

We aim to provide a balance between trainer input, exercises and participant interaction.

Keywords

  • Risk management
  • Risk based approaches
  • Critical processes and study data
  • Key risk indicators

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Course leader(s) & Lecturers

  • Christoffer von Sehested
    Course leader
    Clinical Operations Director
    Nordic Bioscience
  • Sue Gregory
    Course leader
    Director, GCP QA
    KLIFO A/S
See all

IS THIS COURSE FOR YOU?

This course is designed to benefit clinical research professionals who are embarking on implementation of a risk-based approach to clinical trials. Employees working in pharmaceutical and biotechnology companies, CROs and health care sites conducting commercially sponsored studies will benefit from the course.

What you will learn

  1. How to review the basic principles of risk management and utilize them to take a ‘risk-based approach’
  2. How authorities interpret the ICH GCP E6(R2) through review of inspection/audit findings
  3. How to document, prioritize risks and plan mitigation activities and their measurements
  4. How to develop descriptive metrics for your risks
  5. How to identify acceptance criteria and actions
  6. How to review and document your approach
  7. How to discuss methods to communicate and report the approach taken and share best practice

What your company will get

  1. A clinical research professional who understands the principles of risk management and application in a clinical research setting
  2. An employee who will be able to utilize a risk-based approach and define measurable metrics to report on the actual progress for all stages of the clinical trial process from study design, study conduct to study reporting
  3. A professional who can identify and evaluate risks to critical study processes and data and employ mitigation and corrective and preventive action where indicated
  4. A professional who can provide valuable input towards implementation of a risk-based approach across all disciplines within a clinical research unit

Course calendar

Choose your starting date
Starting 14. Dec 2021
Starting 13. Dec 2022
14. Dec 2021 9:00-16:00

DAY 1

  • Welcome and setting the scene
  • Clinical process and data identification + exercise 1
  • Risk identification and evaluation + exercise 2
  • Risk control + exercise 3
  • Risk control + exercise 3 continues
  • Preparation for day 2
  • End of day 1
15. Dec 2021 9:00-16:00

DAY 2

  • Recap on day 1
  • Risk review + exercise 4
  • Risk communication and risk reporting
  • Risk communication and risk reporting + exercise 5
  • Kahoot and wrap up
  • End of day 2
Practical information

Registration

Registration deadline
7. Dec 2021
Atrium
Lersø Parkallé 101
2100 København Ø
13. Dec 2022 9:00-16:00

DAY 1

  • Welcome and setting the scene
  • Clinical process and data identification + exercise 1
  • Risk identification and evaluation + exercise 2
  • Risk control + exercise 3
  • Risk control + exercise 3 continues
  • Preparation for day 2
  • End of day 1
14. Dec 2022 9:00-16:00

DAY 2

  • Recap on day 1
  • Risk review + exercise 4
  • Risk communication and risk reporting
  • Risk communication and risk reporting + exercise 5
  • Kahoot and wrap up
  • End of day 2
Practical information

Registration

Registration deadline
6. Dec 2022
Atrium
Lersø Parkallé 101
2100 København Ø
Sometimes things change. This is the expected programme.

Course information

Literature

Prior to the course you will get access to mandatory and optional readings via your personal Atrium log-in.

Please familiarize yourself with the mandatory readings before starting the course.

Examination

There is no examination for this course.

Course leader(s)

Christoffer von Sehested
Clinical Operations Director
Nordic Bioscience
Sue Gregory
Director, GCP QA
KLIFO A/S

Lecturers

Christoffer von Sehested
Clinical Operations Director
Nordic Bioscience
Sue Gregory
Director, GCP QA
KLIFO A/S

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WANT TO KNOW MORE or need help?

Contact Client Manager Christina Spangsberg at +45 39 15 09 22

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