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Virtual

Nov 18, 2020 1:45 PM - Nov 19, 2020 7:00 PM

(Central Europe Standard Time)

Clinical Trial Regulation Conference

Join experts from regulatory, ethics bodies, sponsors and patients to discuss latest developments of Clinical Trial Regulation and ensure its successful launch.

Session 5: 1 Year Countdwon: Are You Ready? Or What is Needed? Member States Perspective/Feeedback

Session Chair(s)

Elke  Stahl, PhD

Elke Stahl, PhD

Senior Expert, Clinical Trials Department

Federal Institute For Drugs and Medical Devices (BfArM), Germany

Session 5: 1 Year Countdwon: Are You Ready? Or What is Needed? Member States Perspective/Feeedback

Speaker(s)

Elke  Stahl, PhD

CTFG Traffic Light

Elke Stahl, PhD

Federal Institute For Drugs and Medical Devices (BfArM), Germany

Senior Expert, Clinical Trials Department

Greet  Musch, PhD

Readiness in Belgium

Greet Musch, PhD

FAMHP, Belgium

strategic adviser

Ann Marie  Janson Lang

Readiness in Sweden

Ann Marie Janson Lang

and Coordination Group (under Heads of Medicines Agencies), Sweden

Medical Products Agency (MPA) Co-Chair, Clinical Trials Facilitation

Lene Grejs  Petersen

Readiness in Denmark

Lene Grejs Petersen

Danish Medicines Agency, Denmark

Senior Adviser, Clinical Trials

Stefan  Strasser, MD

Readiness in Austria

Stefan Strasser, MD

AGES, Austria

Head of Clinical Trials, Institute Surveillance

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