Adhere to new clinical data disclosure regulations from the US and EU by understanding all parts of the transparency process and avoiding public misunderstandings and penalties.

The CTIS regulations alongside FDA regulations has given the clinical data disclosure and transparency landscape a renewed interest for professionals and requires a space for discussing best practices regarding global regulations going forward. This summit will explore how to quickly create experts in any sized organization on these clinical data disclosure policies and discover how to be confident in earlier disclosure of clinical trials.

TOP REASONS TO ATTEND:
– Achieve elevated confidence in clinical disclosure practices for US and EU standards on both a company and team level.
– Construct a transparency team that will allow efficient clinical data disclosure practices for internal and external relations.
– Discuss how to prepare clinical data for disclosure in the earliest and most compliant way to appeal to all governments involved in regulation and compliance.
– Guarantee compliance documents are future proofed for disclosure compliance and protection.
– Understand clinical data disclosure enforcement and how to best avoid penalties.

DATES & VENUE
15 Feb - 16 Feb 2023, 9:00 am - 2:00 pm
#_REVIEWS

OTHER INFORMATION
Go to Event Website
Ticket pricing starts from:
Pharma/Med Devices/Biotechnology Companies - Standard: USD 995.00
TOPICS | CATEGORIES






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