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ClinicalRM (Clinical Research Management, Inc.) is a full service CRO offering a complete range of management and technical support services in the areas of clinical research support, clinical data management, statistical support, and regulatory support to both commercial and government clients. CRM specializes in technical writing and publishing of regulatory documents including pre-investigational new drug (IND) packages, IND applications, annual reports and IND amendments. They offer quality control evaluation of regulatory documents to ensure consistency and accuracy prior to FDA submission. CRM has provided long-term support and collaboration to client research facilities, including clinical trials centers, pre-clinical research laboratories and a bio-production facility manufacturing under good manufacturing practice (GMP) standards. GMP manufacturing includes quality control testing, and final product formulation/filling. CRM has also collaborated with third-party facilities for conducting outsourced clinical trials in collaboration with clients.