7th Annual Clinical Data Disclosure, Transparency & Dissemination is part of the Informa Connect Division of Informa PLC

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January 22-24, 2020
Orlando, FL

Global Disclosure Mandates • Data Sharing • Plain Language Summaries • Data & Document Anonymization • Medical & Regulatory Writing

As global regulations and requirements continue to evolve, join us at CBI’s 7th Annual Clinical Data Disclosure, Transparency & Dissemination conference to stay ahead of the curve and benefit from critical insights from industry leaders and regulators. Gain insights on emerging regulations, benchmark against your peers and enhance your understanding to enhance compliance in clinical trial disclosure and transparency. Convening trials sponsors, researchers and experts across the field, this comprehensive program delves into the processes and ethics around plain language summaries, data anonymization, regulatory and medical communications writing, resource allocation and much more. From exploring new FDA pilots and initiatives to hearing updates on EU Policy 0070, ICMJE requirements and regulations in emerging markets, this program provides essential knowledge for clinical professionals.

Take Advantage of our Advanced Pricing Discount...

Register by December 6th, 2019 and Save $300!

New for 2020

Expanded Content on Emerging Regulations, Plain Language Summaries and Medical Writing!

KEY INSIGHTS & TAKEAWAYS:
  • Prepare your organization for Health Canada Implementation
  • Gain insight on stakeholder perspectives of Clinical Data and Data Sharing
  • Explore global regulations and guidance’s effect disclosure and transparency
  • Identify strategies to come together as an industry amid regulations
2020 PROGRAM FEATURES:

3 IN-DEPTH TRACKS

  • Disclosure & Transparency
  • Plain Language Summaries & Dissemination Strategies
  • Regulatory & Medical Communications Writing


PLUS...

  • 3 Days of Comprehensive Programming
  • 9 A-la-Carte Breakout Sessions, Skills Labs and Working Groups for a Customized Conference Experience
  • Regulatory Perspectives & Keynotes focused on evolving regulations and initiatives from the EMA, FDA and Health Canada
  • Streamline Processes to Manage Diverse Disclosure Requirements and Updates
  • Elevate Patient and Caregiver Engagement through Improved Access to Clinical Information