Addressing IDMP System Requirements with TrackWise and Navitas
Webinar for Pharmaceutical Companies

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.

In advance of EMA's final IDMP guidance, Sparta Systems and Navitas have partnered to ensure organizations are prepared for implementation by offering an integrated solution: idmpREADYTM

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.

Scott Mitreuter, Product Management, Sparta Systems

David Gwyn, Product Management, Navitas

Areas covered in the Webinar:

  • FDA and ISO requirements for IDMP
  • Establishment of an IDMP strategy
  • Develop a solution to meet the new IDMP regulations
  • Integration between Sparta Systems' TrackWise and Navitas

Who will benefit:

This webinar will provide insight for pharmaceutical companies on building a strong solution to meet the regulatory requirements of IDMP. The people who will benefit include:

  • Regulatory and Compliance Management
  • QA Management
  • Quality System Auditors
  • Consultants


David Gwyn
Head - Content Management & Collaboration

Scott Mitreuter
Product Management
Sparta Systems

Date and Time:
Thursday, September 22, 2016
11am ET / 8am PT

Please fill the form to Register!

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