Trusted technology vendors offer purpose-built tools to help sponsors and CROs meet ICH E6 (R3) and E8 guidelines, improving patient safety and speeding time to market. We’ve vetted the best options to simplify your path to compliance. Our expert team matches your needs with CRF Part 11 compliant solutions—from RBQM and vendor oversight to data visualization and regulatory reporting. With AI-powered insights, you can spot risks early and stay ahead in trial execution.
E-Clinical Agency's strategic tech solutions include:
Cyntegrity MyRBQM – An end-to-end RBQM approach combining AI-powered risk based monitoring and a proven implementation model—empowering teams to manage clinical trial risk efficiently, compliantly, and at scale.
Cencora PharmaLex psiXchange – Fully automated intake and distribution of SUSARs and other safety documents from any system, with real-time tracking, full audit trails, and seamless integration into existing workflows.
Strategikon Clinical Maestro – A single platform that unifies budgeting, sourcing, and contract management—delivering faster RFPs, more accurate budgets, and substantial cost savings across the clinical trial lifecycle.
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