In regulated environments, document management and control is essential to an effective quality management and regulatory compliant system. Managing your documents with InfoStrength SES ensures compliance with regulatory standards.




Improve communication and teamwork across departments and functional areas with integrated collaboration and workflow tools. Infostrength makes it easy to globally access, create, modify, approve and electronically sign documents.

 

InfoStrength is a 21 CFR Part 11 compliant SaaS solution that supports document, regulatory, quality, and risk management systems for medical device, pharmaceutical and biotech companies during the commercialization process.