07/17/2018
As technology regulations and requirements evolve and into a sustainable infrastructure for data management and organization, our standards tone themselves. We enable our clients to show control over their in environments so that they are always audit-ready.
"IDMP (identification of medical products) regulation supports EU terminology for products, substances, and organizations in order to power pharmacovigilance and systems.
In this, they hope to improve safety signal detection and response, verify authenticity, address shortages and recalls quickly, and increase regulatory efficiency...
This transition is part of a two-year rollout with adoption mandatory by 2018."
Regulatory Changes on the Horizon: Global Impact of the IDMP Posted: July 6, 2016July 6, 2016 by Raymond Glemser Categories: Industry Views Share Pharmaceutical manufacturers and CROs face increasingly complex regulatory mandates on the horizon. As requirements increase, so do opportunities for pr...