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What You Need to Know About Submitting eCTD Advertising Promotional Materials

What You Need to Know About Submitting eCTD Advertising Promotional Materials
02 February 2018

Join our Senior Regulatory Affairs Manager, Thomas Christensen, at the Regulatory Submissions, Information, and Document Management Forum in North Bethesda, MD, for his eCTD AdPromo Panel Discussion on February 6, 2018 from 11 a.m. – 12:15 p.m. EST.

While the electronic common technical documents (eCTDs) AdPromo Guidance from the FDA has been out for more than two years, many companies have yet to switch to the eCTD process. Several of them find the process complicated, expensive and time consuming.

In the discussion, Thomas will provide his insights on what to expect when making the switch to submitting AdPromo materials in eCTD format. Attendees will leave the session with an understanding about the submission process and will be able to anticipate the potential challenges that may come when changing from a legacy process.

The three-day forum is presented by the Drug Information Association and provides multiple opportunities for networking, knowledge sharing, and education for both business and technology focused attendees. Click here to learn more about the event, or contact us at Synteract if you need support for your clinical trial, data management and submission needs.

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