Location: Raleigh, North Carolina
Seeking a software solution to integrate the various responsibilities of its regulatory programs. This solution must encompass the primary duties of each of the sections regulatory programs which are Inspections, Sampling, Product Registration, Label Review, Incident Tracking, and Investigations. As each of these programs may involve products and/or manufacturers that cross into more than one program, this solution must be fully integrated across the various programs. The new solution must also provide a public portal to allow registrants to register, and maintain products, and make online payments.
The new system must align our programs with the standards established by FDA under the grant. We expect to go live with all phases of the project by July 2020.
|Considerable knowledge of reporting using SSRS.||