🎉 Thank You for attending Clinical Data Disclosure US 2024! On-demand is available until Friday 12th April! ⏰.
The presentation recordings are now available on ConnectMe until Friday 12th April! After this, the presentations will be available on our streamly video platform for 12 months. Mark your calendar to join us at our Euopean event, 7-8 November, 2024! Sign up for email updates below and check out our full calendar of upcoming events at: https://informaconnect.com/clinical-trials-series/
18 - 19 March, 2025,
Hybrid Event I Attend Live In-Person or Online
THANK YOU FOR JOINING US IN 2024! CLINICAL DATA DISCLOSURE IS BACK AGAIN IN PHILADELPHIA IN 2025!
Stay Tuned for the Upcoming 2025 agenda: Deliver a roubst data diclosure strategy with practical advise.
Benchmark, Be Inspired And Prepare To Meet Regulatory Mandates With Fellow Industry Professionals.
We hope that everyone has enjoyed the ConnectMe experience!
Attendees benefited from:
🏅 Building their attendee badge
👥 Conncted and searched for other attendees; filtering by name, company, interests, and attendee type
📲 Supercharged Their Profile! 🎯 Used Filters to Showcase Their Story & Turbocharge Networking
📽️ Viewed Exclusive 2023 Clinical Data Disclosure Europe Featured Video Highlights
For any ConnectMe Queries, please reach out to: Katie.Condon@Informa.com
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Critical Discussions Shaping the Landscape of Clinical Data Disclosure & Transparency
Protect your Data and Company Confidential Information (CCI)
- Legal considerations resulting from CTIS and EU CTR: from GDRP to CCI
- How to proactively manage CCI in documents
- Experience of retrospective redaction for transition studies
- Implications of the European Health Data Space
- Policy 0070 re-start: ensuring participant’s privacy is protected
Achieve Compliance Whilst Safeguarding Your Organization
- Practical experience of the CTIS submissions process and transitioning trials
- Requirements for Lay Protocol Synopsis & Plain Language Summaries (PLS) of Results
- EMA Clinical Data Publication Policy 0070
- ClinicalTrials.gov modernization efforts
Benchmark & Discuss Your Practical Approaches to...
- Handling RFIs: experiences, expectations, and resources
- How sponsors can utilize and leverage AI
- Managing workload: resourcing, integrating new staff, and solutions
- Feedback on plain language results summaries
- Efficiency savings by utilizing synergy between EU CTIS and ClinicalTrials.gov
Deliver A Robust Data Transparency Strategy With Practical Advice From A Dynamic Speaker Line-Up
Regulatory Authorities, Pharma and Biotech Companies, CROs, and Vendors
Connect with Key Decision-Makers at Clinical Data Disclosure, Transparency & Plain Language Summaries
Whether you're increasing your company profile, launching a new product or focusing on new business development opportunities, collaborate with us to identify custom solutions to help you reach your goals.
Contact Kristen Schott: kschott@informaconnectls.com