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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.
Explore and understand clinical data disclosure enforcement to avoid penalties.
Discuss FDA’s responsibilities related to clinicaltrials.gov, challenges related to the EU-CTR and CTIS transition, disclosure process and more.
Participate in panel discussions and keynote sessions to achieve elevated confidence in clinical disclosure practices for US and EU standards.
Listen to top industry leaders to prepare clinical data for disclosure in the most compliant manner to meet all regulatory and compliance standards.
With 100+ years of combined leadership experience, Momentum proudly serves our clients and produces live and virtual events that attract the best and brightest minds who come together to share their knowledge, connect with the individuals that matter
Offering flexibility, in-depth regulatory knowledge, and technical expertise in the area of Transparency and Clinical Trial disclosure, Xogene offers quality outsourcing of transparency activities, management consulting, and technology-driven solutio
Since 2004, Kateric has been partnering with global biopharmaceutical companies to provide individualized, single source solutions for the preparation of a wide array of regulatory documents.
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