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?

  • 10. Nov 2020

1 day course


5.400,- DKK ex VAT
(app. 726,- EUR ex VAT)


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"



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

Course calendar

Start 10. Nov 2020
10. Nov 2020
Registration deadline 3. Nov 2020

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
Available start dates

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

If you cancel your registration more than 30 days prior to the course, you will receive a full refund. If you get sick and cannot attend the course, you may hand over the seat to a colleague, who will then have to register for the course on our website prior to course start. If the registration is closed, please send us full name, email, phone and title of your colleague to bfl@atriumcph.comRead our cancellation policy.


Contact Coordinator Christina Spangsberg at +45 39 15 09 22

Send an email


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