'Serious adverse reporting system' trends

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1vsoftinfo.com
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The ClinForce system, a web based application, offers the maximum flexibility for creating the design. ClinForce optimizes the subject enrollment and drug inventory and provides access to the system in multiple languages. The built in controls and checks provide management with the confidence required to proceed at a rapid pace. The system complies with regulatory requirements, including 21 CFR Part 11, and CDISC standards. The ClinForce system presents itself as an end-to-end solution for Clinical Trials which includes Clinical Trial Management System (CTMS), Electronic Information Capture (EIC), eDiary/ePRO, Randomization, Clinical Drug Labeling, Randomization Administration(IVRS-INTERNET), Safety Surveillance, VReport System, VDataware

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