This co-hosted webcast between Sparta Systems and Navitas provides an overview of the FDA Guidance for the recent IDMP regulation and explains 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.
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.
Presenters:
Gary Aldam, Senior Consultant, Navitas
David Gwyn, Product Management, Navitas
Joe Humm, VP Sales Operations, Sparta Systems
Scott Mitreuter, Product Management, Sparta Systems
Areas covered in the Webcast:
- 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 webcast provides 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