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Skip to main content User account menu Log in Create Account Search Main navigation New to CDISC Academic Researcher BioPharma Patient Foundation Regulatory Agency Technology/Software Developer About Standards Foundational BRIDG PRM SEND CDASH SDTM SDTMIG ADaM QRS Medical Devices PGx Data Exchange CTR-XML Dataset-XML Define-XML LAB ODM-XML RDF SDM-XML Terminology Glossary Controlled Terminology Therapeutic Areas Alphabetical By Disease Area Published User Guides Standards Publications In Development Public Reviews Standards in Development Real World Data CDISC 360 CDISC Library CDISC Library Archives Education Featured Courses ADaM Core Theory and Application CDASH Advanced Topics SDTM Advanced Topics All Courses Classroom Training Virtual Classroom Training On-Site Training Public Training Instructors Workshops CDISC for Newcomers CDISC Library Workshop Online Training My Learning Course Catalog Upcoming Webinars Blended Learning ADaM Core Theory and Application CDASH Implementation SDTM Theory and Application Support Calendar of Events Contact Us Information for Learners Certification Resources News News What's New For the Press Video Library Annual Report Global Americas Africa Asia Australia Europe Translations Chinese Japanese Stakeholders Global Regulatory Requirements Cases for Clear Data Partner Organizations 3C User Networks Volunteering at CDISC Volunteer Spotlight Become a Volunteer Services ODM Certified Products ODM Benefits and Rates Become ODM Certified Knowledge Base Articles Examples Collection Known Issues eCRF Portal CDISC Primer Guiding Principles Events Conferences 2021 Japan Interchange 2021 China Interchange 2021 US Interchange 2021 Upcoming Events All Events Calendar Partner Events Membership Become a Member Membership Application Benefits & Rates Our Members Learn More Greater Clarity Starts Here CDISC Education Join Us CDISC Membership A CDISC EVENTS EXCLUSIVE PRESENTATION Europe Interchange Keynote Presentation from Dr. Peter Marks, FDA Watch the 2021 Europe Interchange’s final keynote address featuring Dr. Peter Marks, Director, Center for Biologics Evaluation and Research (CBER), speaking on, “ Facilitating the Development of COVID-19 Vaccines. ” Access to all recorded Europe Interchange presentations are available to attendees for one year after the event. CDISC EVENTS Standards Access CDISC end-to-end Foundational and Therapeutic Area standards What's New Stay informed on the latest news, public reviews and standards updates Education Expand your knowledge by attending a global public, private or online training Events Join us at one of our global events to discuss expertise, best practices, and lessons learned in developing and implementing CDISC standards Membership Join over 500 organizations from around the world that support the CDISC vision and mission About Find out what we do and how and why we do it Global Regulatory Requirements CDISC Standards are now required for regulatory submissions to FDA (U.S.) and PMDA (Japan). Learn More CDISC Around the Globe Americas Africa Europe Asia Australia Use Cases for Clear Data Learn how organizations have applied CDISC Standards to bring clarity to data. Learn More CDISC on Twitter Tweets by CDISC Members around the globe /membership/our-members Clear Data. Clear Impact. Footer menu Contact Bylaws & Policies Global Regulatory Requirements Become a Member CDISC and Member Job Opportunities Volunteer Stay Informed © 2021 Clinical Data Interchange Standards Consortium...
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