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Meet your pharmaceutical publication planning challenges head-on with our solution that speeds up processes by 10x+ and closes compliance gaps.
Build custom applications tailored to your unique process – not your competitor’s – using our low-code platform and pre-built workflow components like automated reviewer assignments and debarment checks. Keep processes on track and in the right person's hands with predictive analytics and intelligent routing and approvals.
Meet compliance needs with always-on audit tracking and other validated system capabilities, including FDA 21 CFR Part 11 certified electronic signatures, authority checks, user permissions and access management, and more.
From research concept approvals to publication review processes, applications built on Process Director are 50% lower in cost than incumbent solutions and can be tailored to your unique workflows for optimal efficiency and speed.
With BP Logix’s low-code Process Director platform, Janssen Pharmaceuticals was able to build more user-friendly and compliant workflows for their publication planning process.
"The new system has solved 99% of our compliance issues."
Get in touch with BP Logix to schedule a free demo customized to your organization's needs.
