C-HIT Awarded Follow-on Contract for Supporting the FDA’s Safety Intake Processing Program
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.
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.
