Generation and value of Real World Evidence (RWE)

How can your company make use of the large amount of Real World Data available to generate evidence to support development, market access and safety surveillance?

  • TBD

1 day course

English

5.200,- DKK ex VAT
(app. 699,- EUR ex VAT)

At the moment there are no available dates for this course.

Summary

This course will provide you with an understanding of how Real World Evidence (RWE) can complement evidence from randomized clinical trials and market research. You will learn how to choose study design and data sources depending on the purpose of the study and how you may avoid or limit the impact of the sources of error in observational research.

You will learn about the boundaries between interventional clinical trials, observational clinical studies and market research and the regulatory requirements for the different categories. And you will be introduced to health economics and the importance of this discipline in the pharmaceutical industry. Finally, we will provide an overview of how to protect data privacy when working with healthcare data.

This course replaces the course "Non-interventional studies"

   

Keywords

Real World Data (RWD)
Real World Evidence (RWE)
Epidemiology and pharmacoepidemiology
Observational studies
Non-interventional Studies
Health economics
Market access
Protection of private data

What you will learn

  1. The different opportunities of Real World Data, sometimes called ’Big data’
  2. How Real World Evidence differs from evidence from randomized clinical trials
  3. How to generate Real World Data or use already existing Real World Data
  4. How to apply pharmacoepidemiological methods in observational (non-interventional) studies
  5. How to identify and handle sources of error in observational studies
  6. An understanding of the role of health economics in the pharmaceutical industry
  7. How to comply with the data privacy legislation ‘Persondataloven’ when collecting or analyzing Real World Data

What your company will get

  1. An employee who understands the many different aspects of Real World Evidence (RWE)
  2. An employee who understands the pros and cons of various designs of studies generating RWE and give input to study designs for various study objectives
  3. An employee who can analyze and evaluate pharmacoepidemiological aspects of observational studies
  4. An employee who can identify sources of error
  5. An employee who has an understanding of the impact of health economics and knows how to protect personal data when handling Real World Data

Registration quick facts

You can pay by credit card or by invoice. We charge the amount shortly after you register. If you cancel your registration more than 30 days prior to the course, you will receive a full refund. Read our cancellation policy.

Yes, if you experience any technical problems, please call us at + 45 39 27 60 60, or send us an email at contact@atriumcph.com

If you cancel your registration more than 30 days prior to the course, you will receive a full refund. If you get sick on the day of the course, you can hand over your seat to a colleague. To hand over your seat, please contact us at +45 39 27 60 60. Read our cancellation policy.

Want to know more about this course?

Contact Programme Director Gitte Hornemann Møller at +45 39 15 09 20

Send an email

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