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Joel Finkle

Joel Finkle is Director, Regulatory Innovation and IDMP Strategy for ACUTA. In this role he brings new technologies and regulatory data standards to ACUTA's bio/pharmaceutical customers to ensure compliance and process improvements. Currently, this involves bringing the IDMP (Identification of Medicinal Products) and eCTD (electronic Common Technical Document) version 4.0 standards into our products and services, as well as providing the focal point within the company for other industry standards and regulatory guidance.
Mr. Finkle comes from a background in the Pharmaceutical industry and with software and consulting vendors, with over 30 years experience in software development and support of electronic submissions, publishing, and document templates, from custom CANDAs through eCTDs. He is currently a member of the HL7 Regulatory/Clinical Information Management group, IRISS, and the DIA Cross-SIAC EDM Reference Model team.
He also makes a killer tomatillo salsa.

 Webinar Id: LSHCJI001
12.30 PM PT | 03.30 PM ET
 Duration 60 mins

IDMP data collection from documents - Strategies towards IDMP compliance.

This session will review the basic requirements of the initial planned European implementation of the ISO IDMP standard, then explore how the data for a product could be gathered for entry into a RIM system or what is expected in the agency web portal. Benefits of integration in a RIM environment, and downstream use of the data, will be covered.

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       Single Attendee
(Only for one Participant)
Multiple Attendee
( 2 - 5 Participants)
Corporate Attendee
( 6 - 10 Participants)
(6 months unlimited access)

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