ProEDC®

By collaborating with industry experts on advanced technologies, we find simpler still most effective ways to manage research data. ProEDC® is a way to empower data analytics in research industry. ProClin offers a unified server-based EDC system, serving a broad range of user types and offering full- and self-service. opportunities. The ProEDC Tool is adaptable for:

Studies in any:

  • Therapeutic Area.
  • Trial category, including medical device.
  • Study phase, early to late phase clinical trials.

Research from :

  • Company Sponsors.
  • Clinical Research Organizations.
  • Academic Research Organizations.
  • Investigator-Driven Programs.
  • Public Health Studies.
  • Government Supported Studies.

Functions that :

  • Span studies from startup to submission.

ProCTMS®

Clinical trials are an enormous undertaking. They can involve thousands of people, hundreds of investigative sites, multiple CROs, and various eClinical source systems — all generating massive amounts of data.

ProCTMS® is a powerful end-to-end clinical trials management solution that brings control, efficiency, and quality data to every study. This web-based CTMS works on the go, letting you view and manage real-time operational performance — wherever and whenever.

Support Assets : ProCTMS® makes it easy to connect to clinical trial data through Excel and collaborate in a secure way using direct connection to common folder Bi-directional information exchange between ProCTMS® and Common Folder is seamless, making for a powerful, high-performance solution.

Better Workflow, Deep Savings : With ProClin, you can vastly improve efficiencies in both data flow and workflow, yielding cost savings in time, labour, and operational expenses.

Moreover, integrating Office processes with clinical operations can reduce back-office paperwork and significantly lower administrative overhead. Easy to learn and use, ProCTMS® is quickly mastered, which speeds user adoption. It is mobility enabled in support of the one-of-its-kind offline Monitoring Visit Report (MVR) module, allowing operational performance to be viewed and managed across programs and studies in real-time via secure role-based web access.

Whether 10 users or 1,000, ProCTMS® quickly scales, bringing workflow efficiencies and standardized tracking across all studies of every type, in both online and offline modes. Benefits of the full-featured and configurable ProCTMS® become especially apparent in high volume global programs, yet it is an affordable CTMS solution for organizations of any size.