Harmonized Medical Records, Data Management and Clinical Trial Support and outsourcing both for compliance and application for approval and for the various trial stages in Animal and Human Models, all need efficiency, security and seamless administration across the Clinical Records, and Trial Results Micro and Macro Data Ecosystems.

HMR Is your Solution for today's complex regulatory atmosphere, where speed and quality go together with compliance and accuracy.

HMR Outsourced Clinical trials for new drug Applications in accordance with the CGMP protocols as established by the FDA and the USP standards, is the core support that HMR offers clients, with confidentiality and ethical management of client data.

Contact HMR today for your Outsource needs and we will match and manage your requirements to the highest standards.