Webinar: Regulatory Information Management Made Easy with TrackWise and IDMP Ready

 Wednesday, Sep 12th

 9:00am EDT
 2:00pm BST / 3:00pm CEST

This webinar will provide an overview of the FDA Guidance for the recent IDMP regulation and explain how pharmaceutical companies should prepare and build a solution to meet the IDMP specifications that are connected to the TrackWise system.

idmpREADY combines Navitas' data management technologies to capture, record, publish and maintain IDMP data points, together with Sparta's TrackWise QualityConnect framework to define, track, exchange and report IDMP core processes.

  • Brandon Henning, Product Management, Sparta Systems
  • Tom Beatty, Product Management, Navitas

Areas covered in the Webinar:
  • FDA and ISO requirements for IDMP
  • Develop a solution to meet the new IDMP regulations, including IDMP Submission and eCTD
  • Document Management using PharmaReady and IDMPReady software solution

Who will benefit:

This webinar will provide insight for pharmaceutical companies on building a strong solution to meet the regulatory requirements of IDMP. 

Register Today

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Tom Middleton

Solutions Architect

Sparta Systems

Tom has a passion for helping people ensure management system quality and robust compliance through value-added, process-driven programs. His experience includes standards and regulations for the automotive, life sciences, medical devices and consumer product verticals, including ISO 9001, ISO 13485, ISO 14000, FDA 21 CFR 820, Japanese Pharmaceutical Affairs Law (JPAL), Canadian Medical Devices Conformity Assessment System (CMDCAS), EU Medical Device Directive (MDD), and the Brazilian ANVISA standards.

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