From the Food and Drug Administration (FDA) to the European Medicines Agency (EMA), numerous agencies around the world impose their own sets of regulations on pharmaceutical, health sciences, and biotech firms. LogicGate helps you put the processes in place to remain compliant, such as field force monitoring and biosecurity assessments.
In addition to governmental laws, numerous industry best practices govern drug development and manufacturing, such as CGMP and ISO standards. LogicGate offers solutions that help ensure these best practices are followed through agile controls management.
Given the ever-evolving landscape of medicine, change management is a required component of any proactive governance, risk, and compliance program. LogicGate's automated platform assists with the effective identification, management, and implementation of necessary changes, keeping your organization prepared for what's next.
- Head of Risk and Compliance, Healthcare
Find out how the LogicGate platform leverages cutting-edge technology to automate your governance, risk, and compliance processes.
LogicGate helps build efficiency, oversight, and responsiveness into your entire compliance management program.
Requesting a demo is free and easy. Get in touch and we’ll show you how it works.
Request A Demo