Perceptive eClinical
Clinical Trial Solutions
Effective RTSM, built on 30 years of experience
Backed by the industry’s most experienced designers and RTSM specialists, you can rely on Perceptive eClinical to deliver optimized randomization and trial supply management (RTSM) strategies that keep trials on track, even when they don’t go according to plan – and they never go according to plan.
4.7K
Trials
2.6M+
Patients
500+
Approvals Supported
250+
Adaptive Trials
Evolving and Innovating IRT
Having evolved from its early beginnings as ClinPhone™, Perceptive eClinical’s RTSM is a robust and adaptable platform designed to tackle any challenge. Since 1993, the world’s leading biopharmaceutical companies and CROs repeatedly turn to Perceptive eClinical to meet their RTSM needs. That’s 30 years of experience built into the technology, processes, and people who understand what’s needed to remove RTSM burdens and reduce your trial risks.
Any design. Any complexity.
Perceptive eClinical’s core of pre-validated RTSM functions are designed to support all trial needs, covering study, site and subject management, randomization and dosing, and trial supply management from lot release to destruction. We customize our RTSM system to best meet the needs of each study and protocol. And we match every protocol design, with no limits to the level of complexity we can accommodate. Learn our approach to meeting all your RTSM needs and why you can rely on the expertise behind Perceptive eClinical to help you:
- Optimize Inventory
- Effectively Randomize
- Mitigate Risks
- Improve Planning
- Manage Studies Efficiently
- RTSM Expert Consultancy
Proven. Adaptable. Trusted.
Whether your trial is simple or complex, local or global, with 50 patients or 5,000, you can rely on Perceptive eClinical’s industry-proven RTSM system and experienced professionals to deliver the highest quality solution to drive your trial’s success.
Experience Matters.
Perceptive eClinical’s breadth of experience across all protocol designs, phases, and therapeutic areas translates into a reliable RTSM system designed to meet your trial needs and mitigate risks. Not just the risks you may expect, but those we anticipate. Our RTSM specialists leverage over seven decades of experience to advise how to best implement trial designs and account for planned or unplanned trial scenarios. They work with you to design an RTSM solution based on a comprehensive understanding of your protocol, packaging plan, recruitment rates, and ongoing study needs. The result? An adaptable, flexible, and reliable system ready to meet your current and future trial challenges.
Expert Support for the Life of Your Trial
Our dedicated team of RTSM specialists remain involved in each study until its closure, addressing the inevitable issues you’ll face during the running of a trial, from recruitment delays to drug shortages to protocol amendments.
Do more with your RTSM solution
Trial Supply Management
Effectively Randomize
Study Management
Mitigate Risks
Data Insights
RTSM Expert Consultancy
Our One Pager:
2–4* week study start-up for your simple study designs. Learn more about key benefits and study solutions:
Our eClinical Brochure:
Keep your clinical trials on track and reduce costs. Learn more about potential challenges and how we address them:
