What We Do
There are many common challenges facing clinical trials of all sizes. Among these are:
- Difficulty getting targeted number of sites up and running quickly
- Lower than forecasted patient enrollment rates
- Protocol complexity and limited training opportunities
- Inadequate Informed Consent causing patient dropouts and/or discouraging patient enrollment
Yet, in spite of these challenges, timelines and milestones must be met!
Trifecta MultiMedical has developed a suite of easy to use, easy to implement technology solutions to help study teams overcome these issues and meet or exceed study objectives.
Defining A New Phase
Trifecta MultiMedical is focused on a new phase of the study lifecycle - Site Optimization. Our solutions increase the quality, consistency, and power of clinical trials by improving site operation.
Active Trials
Trifecta MultiMedical’s technology is currently being used on a wide variety of trials—from small, acute care anti-infective studies to rheumatology studies with over 20,000 patients. These studies include the following therapeutic areas:
- Pain & Rheumatology
- Oncology
- HIV/AIDS
- Cardiology
- Respiratory/COPD
- Anti-infective
- Neuroscience
Our Technology
Trifecta MultiMedical utilizes industry best practices for data confidentiality, integrity and availability as defined by the International Information Systems Security Certification Consortium (ISC). With regular review and monitoring of information security controls and processes by both internal and external CISSP Information Security personnel, we take a proactive approach to protecting client data. Application availability is ensured by the use of geographically diverse, redundant data centers utilizing Oracle™ RDBMS.
