Workshop on clinical evaluations and investigations with medical devices

This workshop is arranged by Medicoindustrien’ s Expert group for clinical investigations and kindly hosted by Coloplast.

Only for employees of member companies.

Outcome

The aim of the day is to see what is in the future of the clinical area for medical devices and also meet peers working with clinical evaluations, clinical investigations and post market clinical follow-up and exchange experience.

Program

08.30 – 9.00 Check in & breakfast
09.00 – 9.15 Welcome & introduction
Marie Louise Oemann Mohr, Coloplast
Thomas Krarup Simonsen, Coloplast
09.15 – 10.00 Estimands. ISO14155-2026 now published. Let’s recap estimands,
Charlotte Hindsberger, Coloplast
10.00 – 10.15 Coffee break
10.15 – 10.45 EU in general
Stellan Nørreskov Wulff, Medtech Denmark
Kristian Teglkamp Flemmingson, Coloplast.
10.45 – 11.00 EU specific. Revision of the MDR is in process. Why? And what will (most likely) be revised.
Lene Laursen, Medtech Denmark
11.00 – 11.30 Clinical strategy
Pernille Nonboe, Coloplast. Marked Access
Steffen Nielsen, Coloplast.
11.30 – 12.30 Lunch
12.30 – 13.30 Clinical strategy Continued. PMCF study.
Anna Kaufmann Lindqvist , Novo Nordisk.
RWE Ann-Sophie Iuel-Brockdorff, Coloplast.
13.30 – 14.20 Questions and debate in plenum
14.20 – 14.35 Coffee break
14.35 – 14.55 Danish Ethical Committee news
14.55 – 15.15 DKMA news
15.15 – 15.30 Wrap up & conclusion of the day

Contact

Morten Petersen

Morten Petersen

Uddannelseskonsulent | Training Consultant

49 18 47 03
mp@medicoindustrien.dk

Select date

17. september 2026

17 September 2026 - at 08:30 - 15:30

Price ex. VAT
Member price: Pris ikke angivet
Other: Pris ikke angivet

Latest Registration
05.09.2026
Latest Cancellation
05.09.2026

Address
Coloplast A/S
Holtedam 1
3050 Humlebæk

Register

Terms

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Head of Development
bm@medicoindustrien.dk

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