3rd eRegulatory Submissions Summit

3rd eRegulatory Submissions Summit in Philadelphia on Tuesday, July 9, 2019
3rd eRegulatory Submissions Summit in Philadelphia on Tuesday, July 9, 2019
Tuesday, July 9, 2019 -- Wednesday, July 10, 2019, 0800 - 1700
The Regulatory submissions landscape if ever-changing given the obligatory 2018 initiative to make CTD submissions electronic and the 2019 implementation period required for electronic submission of standardized study data. It is essential to ensure the quality and consistency of each document included in a submission to avoid complicating the regulatory submissions process when multiple team members get involved.

The 3rd eRegulatory Submissions Summit will cover changes made to the electronic submission processes and protocols for constructing strategies for IDMP, RIM, global and regulatory submissions. This summit will also address regulatory information management experiences and the standards for the identification of medicinal products and best practices for eCTD submission requirements.

Top Reasons to Attend:
- Understand the complete regulatory electronic submission process from beginning to end
- Assess the latest developments in ISO IDMP standards and understand the future of data in submissions
- Review the necessities for EDMS Implementation for eCTD system
- Plan improvements to submission processes and ensure communication between all steps in the regulatory submission life cycle
- Discuss time to market strategies and the role of submission management, regulatory project management, and agency interactions
- Gather the essential information needed to publish eCTD
- Explore global and regulatory eCTD management and requirements

Website https://go.evvnt.com/435355-0?pid=2874

Brochure https://go.evvnt.com/435355-3?pid=2874

Prices:
Early Bird USD 1895.0
Standard USD 2095.0
Onsite USD 2195.0

Speakers: Michael Hellerstein Director, Regulatory Affairs and Quality Systems, GEOVAX, Sonja Justice Associate Director, Regulatory Operations, AMICUS THERAPEUTICS, Suzanne Libby Associate Manager, Regulatory Operations, AGIOS PHARMACEUTICALS, Lakshmi Ramkumar Medical Writing Department Head, BOSTON BIOMEDICAL, Deborah Satoh Head of CMC Submissions, TAKEDA , Marc Stern Director, Regulatory Processes, Operations and Publishing, EAGLE PHARMACEUTICALS, Robert Stumpo Director Global Regulatory Medical Writing, TEVA PHARMACEUTICALS
Starting Price Per Person
$ 1895.00 USD
Other Information
Where
Sonesta Philadelphia Downtown Rittenhouse Square
1800 Market Street
Philadelphia 19103
United States
( Hotel - Resort )

                 
Event Organizer Contact
Michael Keogh
mkeogh@questex.com

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Event ID: 152728

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