We are excited to bring together the global standards community through our new, enhanced virtual conference platform. During our flagship event, you will have the opportunity to:

1. Learn from the best in standards implementation through presentations and discussions with our exceptional lineup of speakers.

2. Form valuable connections through our new, enhanced networking experience - share lessons learned and best practices with experts from around the world!

3. Home office friendly. No travel, itineraries or lost receipts required! Access all of our cutting-edge content from the comfort of the environment of your choosing.

4. Build your own agenda and access 24/7 on-demand content. Choose which live presentations you would like to view from one of three tracks. Want to see more than one (or all) live presentations happening at the same time? No problem! All video content will be available on-demand for attendees following the presentations, so you don’t have to miss a thing.

5. 1:1 Virtual Networking. Miss the ability to have a quick meeting? We have a solution! View mutually available times, and schedule a 1:1 video call with another attendee, all available directly through the app.

6. Meet F2F with Exhibitors. Curious about an exhibitor’s specific product or offering, but would prefer to meet F2F with your questions? Enter their Virtual Tradeshow Booth! Exhibitors will be online and on-screen to chat with you about their solutions. Prefer to send them a message instead? Leave them a quick message in their booth, and they’ll get right back to you! Also, make sure to check out our 3D Exhibition experience! 

7. Live Q&A, Live polling, and live chat. No need to find a microphone – ask your questions within the platform through live Q&A, participate in live polls, and discuss hot topics through live chat features. Want to keep the discussion going after a presentation? Check out our sessions-based forums!

Who Should Attend?

Biostatisticians, Clinicians, Concept Modelers, CRF Designers, Data Managers, Decision Makers, Innovators, Medical Writers, Metadata Modelers, Programmers, Study Designers, Study Management, Team Leads

CDISC standards are required for regulatory submissions to the US FDA and Japan PMDA, recommended by the China NMPA, and requested for use by the European Innovative Medicines Initiative (IMI).