Sitrof Technologies offers proven IT and content management solutions that allow Tier 1 and Tier 2 life sciences firms to streamline and automate their regulatory affairs, safety/pharmacovigilance, compliance and quality assurance processes.Learn More
Authoring. Collaboration. Electronic signatures. Title 21 CFR Part 11 compliance. No matter the regulatory hurdle, Sitrof has helped our life sciences clients clear it.Learn More
Sitrof’s adverse event intake automation solutions empower Tier 1 and Tier 2 life sciences clients to reduce human error and centralize essential processes while creating a compliant digital archive of critical data. It’s pharmacovigilance, simplified.
From validated systems to integrated GRC solutions, Sitrof helps leading life sciences firms improve document management and content management practices to ensure compliance with Title 21 CFR Part 11, HIPAA, SOX and more.Learn More
Sitrof solutions allow for simple, secure information sharing between all stakeholders in the life sciences quality assurance process – improving overall performance, regulatory compliance and evaluation.