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Bethesda North Marriott Hotel and Conference Center

2016年2月08日 (月) 午後 12:00 - 2016年2月10日 (水) 午後 5:15

5701 Marinelli Road, , North Bethesda, MD 20852 , USA

Regulatory Submissions, Information, and Document Management Forum

Discuss the end-to-end process for document management, publishing, and technical regulatory requirements in regulatory information management.

戻る Agenda

Session 2 Track 3 - Cloud EDMS Selection, Implementation, and Use Interactive Discussion

Session Chair(s)

Daniel Orfe, MS

Daniel Orfe, MS

President and CEO, Regulatory eSubmissions, LLC, United States

Cloud based EDMS systems are becoming a key driver in the Pharma-Biotech industry. These systems are being used to meet regulatory requirements and provide for organizational efficiency.
This is an interactive session with audience participation. The participants from emerging Pharma-Biotech companies and the session chair will relate three significant benefits and three major considerations (hurtles - errors), based upon each of their organizations experiences.
The session will cover the selection process, implementation efforts, and ongoing use of the cloud based EDMS system. Once background has been provided by the panelists, the audience will be engaged to participate in a highly interactive session.

Speaker(s)

Marc Gabriel

Marc Gabriel

Vice President, Regulatory, Veeva Systems, United States

A Service Provider’s Experience With Cloud EDMS

Ronald Hernando, MBA

Sr. Consultant, Vault RIM Business Process Consulting, Veeva Systems, United States

18 Months (and Counting) of Agony Fixed in 7 Weeks: Implementing a Cloud-Based EDMS

Samuel Collier

Product Integration and Deployment Coordinator, Montrium, Canada

Cloud Based EDMS: Three Pros and Three Cons