Streamline and automate publication planning, research concept approvals, and more with BP Logix's low-code process automation platform for pharma and life sciences: PubPro.
Experience PubPro with our interactive demo:
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, implementing PubPro can result in up to 50% lower cost than incumbent solutions because it's tailored to your unique workflows.
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."