Overview
Tutorial: May 11th
Meeting: May 11th-13th
Virtual Event: Click here for details.
EDM and ERS is combining with RIM in 2015 for the eRegulatory and Intelligence Annual Conference. In recent years, industry as a whole has been converging towards looking at regulatory as an end-to-end process. Document management, publishing and technical regulatory requirements are all subsets of regulatory information management at its broadest definition.
The program committee is developing this conference featuring plenary sessions on latest trends in the industry as well as FDA and other Agency updates for direct dialogue with industry. This conference serves as a forum for the discussion of emerging standards and the processes for submission creation and maximum use of regulatory information. The highly appreciated "Ask the Regulators Session" will be augmented by "Ask the Industry Experts" sessions to provide avenues of two way discussions of hot topics with the Regulators, industry experts and audience participants (questions can be submitted ahead of time).
Sessions are separated into four tracks. The RIM business-focused track provides the opportunity to interact and share experiences related to processes for obtaining and managing regulatory information and the organizational impact as well as gain a greater understanding of key issues shaping the global regulatory environment. The technology track will focus on standards related to submission of regulatory information, the tools necessary to effectively manage the information, and associated implementation experiences and lessons learned. The traditional ERS and EDM tracks will focus on emerging trends and best practices in regulatory submissions and electronic document management, respectively.
As the eRegulatory and intelligence space emerges, it is critical to break down silos for end to end processing of regulatory information as it relates to EDM and ERS. Lessons learned from recent mergers have highlighted the importance of regulatory intelligence as well as efficient systems and processes. Many people and companies define RIM differently but maximizing access to information is critical to gain efficiencies and remain competitive. This year’s new combined program aims to incorporate all relevant topics from the previous separate conferences without sacrificing focus.
This program is being developed in collaboration with the Document and Records Management and Electronic Regulatory Submissions Communities.
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Program Committee
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Christian A. Buckley, MBA, RAC Associate Director, Regulatory Affairs
Astellas, United States -
Sarah Powell, RAC President
Powell Regulatory Services, United States -
Kimberly Belsky, MS Reg Policy & Intell and AdPromo, Regulatory Affairs
Independent, United States -
Jake Doran Head of Digital
Lykos Therapeutics, United States -
Betsy Fallen, RN Consultant
BAFallen Consulting LLC, United States -
Mark A. Gray Senior Project Manager, DSB, CBER
FDA, United States -
Ginny Hussong Branch Chief, Data Standards, CBER
FDA, United States -
Dominique Lagrave, PharmD Senior Vice President of Regulatory Innovation
Accumulus Synergy, United States -
Daniel Orfe, MS President and CEO
Regulatory eSubmissions, LLC, United States -
Emily Onkka Senior Director, Regulatory Affairs
Pfenex, Inc., United States -
Laura J. Sherman, MBA Training Partner, Clinical Business Operations
Vertex Pharmaceuticals, Inc., United States -
Stacy Tegan Program Director
Transcelerate Biopharma, Inc., United States -
Hans van Bruggen, MSc CSO
Qdossier, a Celegence Company, Netherlands
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