TRACK ALL COMPLIANCE, REGULATORY & LOGISTICS
All clinical studies require the development and approval of a protocol, which describes the objectives, design, methodology, statistical considerations, and organization of a trial. The entire process from compliance to regulatory submissions to logistical requirements can be very challenging for any organization. In addition, without the proper application to support the workflow process, tasks, milestones, documentation and requirements can be missed or overlooked by any team.
The CTMS Clinical Tracker provides a centralized repository to manage and administrate the workflow process in order for compliance, requirements, submissions and logistics to be handled, as a multi process engine identifying required tasks to be distributed, shared and completed within a specified time frame. The Clinical Tracker provides collaboration between Sponsors, CRO’s and Sites to simplify the process of understanding and managing the volumes files, documents and requirements for a clinical trial.
For more information about CTMS and Clinical Tracker email GPMS today: CTRAC@globalpmsystems.com