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The role of medical affairs leaders has evolved, especially in bringing new drugs to market. Learn more about those trends and how they're affecting startup pharma companies.
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.
Get in touch with BP Logix to schedule a free demo customized to your organization's needs.
