Life Sciences Industry
Clinical Trial Management
Advance Control and Overview
Our Clinical Trial Management solution meets the requirements of the highly sensitive and regulated market of clinical studies and complies with cGMP/GCP guidelines. The concept of this integrated system focuses both on the efficiency of the application and the safety demands given by regulatory authorities.
RS PMX CTM™ fulfills the specific development requirements of the target industries. It integrates completely into the global enterprise structure, following a modular and object-oriented concept. RS PMX CTM stands for organization of the complete material and information flow from production, randomization, and primary/secondary packaging to delivery, batch tracing, and surveillance of the expiry or retest date of the trial samples.
The solution can be used as both a stand-alone system or an integrated solution interfacing to existing systems such as IVRS (Interactive Voice Response System) and EDC systems (Electronic Data Capturing). With the basic functionality necessary for the clinical supply chain, RS PMX CTM represents an efficient and powerful IT solution.
Case In Point
- Industry client — Leading manufacturer of insulin and diabetes care products
- Objective — Overall management of clinical trial materials with focus on the production of clinical trial study supplies
- Results — Improved clinical trial management by 20% offering shorter time-to-market, reduced operating costs, and preconditioned data for the manufacturing and packaging department