Register™

Drug Registration Tracking Software

Managing and tracking global product registrations and on-going submissions is a time-consuming, repetitive process that requires extensive input from every affiliate and licensing partner.

Register is a comprehensive registration and regulatory submission tracking software that enables you to easily manage and coordinate global registration tracking activities. Register also helps you to maintain critical product data, such as formulations, indications, packaging, release specifications, manufacturing procedures, and other detailed product information required for global regulatory and QA compliance. Register also supports all the required data elements of the EudraVigilance Medicinal Product Dictionary (EVMPD).

Register's intuitive, user-friendly design allows for easy configuration and deployment throughout your organization, giving your regulatory department the ability to meet internal and external demands, while simultaneously managing all of your global registration activities.

Compliant with the latest regulatory guidelines including National, Central and Mutual Recognition Procedures, Register tracks all registration and re-registration activities including registration planning & tracking, management of regulatory/affiliate questions and tracking of variations etc., facilitating overall product management and regulatory decisions.