document management and control for pharmaceutical and medical device companies
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.

electronic signatures for regulatory documents

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.

access your QMS from anywhere
Collaborative tools and content co-exist in an intuitive, web-based environment to enhance your team and community collaboration experience with shared expertise and best practices within your organization and beyond.


create quality and regulatory systems

Create custom configured applications quickly, and share them with your co-workers in real time. Our intuitive wizard guides you in building and maintaining custom applications yourself... no coding required!


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.