Balancing the Benefits and Costs of Research and Clinical Trials Data Transparency: Copenhagen Centre for Regulatory Sciences (CORS)

Aktivitet: Tale eller præsentation - typerForedrag og mundtlige bidrag

Timo Minssen - Foredragsholder

  • JUR Forskningscenterområdet - fordelingssted
Recent US and European initiatives reflect a growing policy consensus favoring greater clinical trials and research transparency. New legislation, publishers and industry-driven projects promote independent verification of drug data, which provides a better framework for international collaboration. Greater transparency also increases public trust in research results, drugs and industry and the possibility of facilitating large cross-border clinical trials. Yet, the costs and concerns associated with opening up research and clinical trial data are also significant—for patients (protection of personal data and patient privacy), for research (misuse of clinical trial data) and for technology transfer and commercialization (obstacles to IP protection and increased exposure to litigation). This presentation will discuss these issues from an interdisciplinary perspective in order to sketch out legal mechanism that could be useful for unlocking and safe-guarding the full potential of greater transparency.
21 apr. 2016

Begivenhed (Konference)

TitelThe Future Directions in Regulatory Science
Dato21/04/201621/05/2016
Hjemmeside
AfholdelsesstedUniversity of Copenhagen, Universitetsparken 2, 2100 Copenhagen, AUDITORIUM A3
ByCopenhagen
LandDanmark
KontekstInternational begivenhed

Antal downloads er baseret på statistik fra Google Scholar og www.ku.dk

Ingen data tilgængelig

ID: 161117891