Nextrove Successfully Hosts MedAssessment on AWS Cloud with Seamless Argus Migration
January 2025
About Nextrove
Nextrove leads the industry in Pharmacovigilance Professional Services and Solutions. Our unwavering mission, “Empowering Clients to Improve Patient Safety,” propels us on the path to realizing our vision of becoming the first choice for Life Sciences professional services and solutions, in service of our clients, partners, and, above all, the patients we ultimately serve.
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Nextrove LLC is proud to announce the successful migration and hosting of MedAssessment, a leading global CRO, onto the Nextrove AWS Cloud. This achievement showcases Nextrove’s commitment to delivering innovative, scalable solutions and exceptional service in the field of pharmacovigilance.
The President of MedAssessment Peg Fletcher, MD, PhD expressed her satisfaction with the project:
"This has been the smoothest migration I have experienced. The professionalism, dedication, and teamwork of the Nextrove team ensured the project’s success from start to finish. We couldn’t have asked for a better experience!"
The three-month project was a collaborative effort between MedAssessment and Nextrove’s dedicated team, including Abhisek, Abhinay, Rudra, Nivedita, Javid, Shalet, and Sumit, whose exceptional contributions kept the project on track.
MedAssessment also praised Nextrove’s proprietary migration methodology for its precision and efficiency, highlighting the seamless execution and the consistent support provided throughout the migration process.
MedAssessment, Inc. is a US-based Contract Research Organization (CRO) specializing in pharmacovigilance and early drug development assessments. They provide a comprehensive range of services including safety monitoring, signal detection, and medical writing to drug sponsors and clinical operations teams. With a dynamic team of multilingual medical professionals, MedAssessment leverages advanced technology to streamline safety data management and ensure compliant regulatory submissions. Their expertise is particularly focused on early-stage clinical trials, aiming to deliver high-quality safety profiles to facilitate faster product approvals.