Meeting Program

Explore the Drug Development Continuum Life Cycle

EDM and ERS/eCTD 2013 conference serves as a forum for the discussion of emerging standards and the processes for submission creation and maximum use of regulatory information. This year’s conference will feature facilitated roundtable lunch discussions on industry hot topics such as how to separate content vs context, eHealthcare, data standards and records management as well as bringing back the Ask the Regulators Session to provide a venue to discuss hot topics with the Regulators and ask the panelists questions regarding FDA submission standards, processes, regulations, guidance, or initiatives (questions can be submitted ahead of time). Please note: Questions for the “Ask the Regulators” Session will be collected onsite; there will be an area at the DIA registration desk for collection.  Questions will be collected Tuesday, October 15th and Wednesday, October 16th.

EDM Meeting Program

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