Regulatory Networking Group

Join a professional community with colleagues from the industry and authorities

  • TBD

4 days course

Danish

4.375,- DKK ex VAT
(app. 588,- EUR ex VAT)

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

If you want to join the network that is running now, please contact Senior Programme Director, Tina Jensen at tj@atriumcph.com  

Summary

As a member of the regulatory network group you are a part of a professional community. The activities are based on exactly the issues that you, as a regulatory professional, face in your everyday life, and you will have the opportunity to learn from and share experience with colleagues, who have practical experience with the issues that you are engaged in.

We offer you four annual meetings, where you as members are the ones who decide which subjects we should address. In 2017 the members had decided on the following subjects:

Falsified Medicines/Serialisation
The new Danish Medicines Agency
Quality by Design
Drug/Device Combinations

As regards to the subjects of 2018 the group will decide on these and our intention is, as we did in 2017, to invite speakers from both the authorities and the industry, where it is relevant. If you want to have a say regarding the subjects to be dealt with – please register no later than 10 January 2018.

What is it about?

The four annual meetings will take place from 15.00 to approx. 18.00. During the three hours we will discuss professional subjects and do some networking exercises, which all together will form a professional and social community of trust and openness.

The contribution from the speakers will frame the following discussion and exchange of experience on the subjects. The networking interaction is a very large part of this network - the possibility to hear how others have handled exactly the challenges you are dealing with, and to share experience. Our intention is to create an environment that encourage and inspire you to form smaller network groups across your companies.

Meeting dates & SUBJECTS 2018:

Monday 7. May at 15:00 – approx. 18:00 - EMA/Brexit with speaker Peter Bachmann, BfArM
Tuesday 12. June at 15:00 – approx. 18:00 - Bioequivalence and Comparability
Monday 10. September at 15:00 – approx. 18:00 - Target Product Profile/Target Labelling
Thursday 8. November at 15:00 – approx. 18:00 - Ethical considerations/API Manufacturer, CMOs, GMP-production
 

Keywords

Networking
Sharing of experience
Competent feedback
Discussions
Update on Hot Topics

What you will learn

  1. The opportunity to stay up to date on current topics in the fields of regulatory affairs
  2. The opportunity to discuss challenges with other regulatory affairs experts
  3. The opportunity to expand your network with other regulatory affairs professionals
  4. The opportunity to discuss with, share experience with and get inspired by regulatory colleagues from both industry and authorities

What your company will get

  1. An employee who regularly receives new information to aid their daily work with regulatory affairs
  2. The opportunity to discuss challenges with other regulatory affairs experts
  3. An employee who gets inspiration to solve relevant challenges

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 Senior Programme Director Tina Jensen at +45 39 15 09 14

Send an email

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