CTMS solutions for the entire product development lifecycle
Because improving time-to-market for new drugs and devices is critical for life sciences companies, managing the clinical trial process is one of the most significant areas of opportunity for improvement. Often paper-based and always subject to intense regulatory pressure, clinical trials involve managing massive amounts of documentation between multiple parties and systems. Perceptive Informatics’ Clinical Trials Management System (CTMS) streamline and secure the collection, aggregation, and reporting of all non-clinical trial data simultaneously boosting both trial productivity and patient safety.
Our suite of CTMS solutions enable life sciences companies to increase trial productivity, decrease administrative costs, improve patient safety, and increase regulatory compliance. Our solutions accurately, efficiently, and securely manage many aspects of a clinical trial – regardless of size, scope or phase – enabling clients to improve process planning; standardize data collection; more effectively manage both patient and non-clinical data; and improve FDA compliance. Our CTMS solutions include:
IMPACT® - is the world's most used enterprise wide CTMS, with over 25,000 end users and with product modules for managing trial progress, planning, monitoring activities, supplies and cost tracking. IMPACT supports the full spectrum of clinical trial activities, from first-in-man through to marketing studies – and from single site to large-scale, global studies.
INITIATOR™ - is specifically designed to handle the rapid, high-volume nature of Phase 1 unit management.
INVESTIGATOR™ - offers control of investigator information and facilitates the selection of the best investigators and sites for a study.
For more information, please visit the CTMS section of PAREXEL’s Perceptive Informatics’ website, or contact Perceptive Informatics at info@perceptive.com or call 1 866 289 4464.