C-HIT is pleased to announce that the Food and Drug Administration (FDA) Office of Office of Information Management and Technology (OIMT) has selected us to continue providing operations and maintenance support for the FDA’s Safety Intake Processing Systems (SIPS) program. C-HIT’s Contract scope also entails modernizing and enhancing SIPS and individual subsystems – Safety Reporting Portal (SRP), MedWatch, and Global Substance Registration System (GSRS). These component systems are critical for reporting observed or suspected adverse events and problems to the FDA, while requiring high availability with limited scheduled downtime.
C-HIT had been supporting this program for more than a year previously, providing O & M services that included operating these three separate and distinct subsystems under one program while identifying ways to maximize efficiencies through shared services. “C-HIT is honored to have been awarded this follow-on program by FDA. To us, it shows that the Agency values the experience and skills our team brings to the program,” stated Dr. Srivasavi Chaganti, C-HIT President and CEO. “We remain committed to partnering with FDA and delivering quality services, innovative technologies, and cost efficiencies on the SIPS program,” she added.
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