Sitrof Technologies solves the most challenging IT and content management issues in the life sciences industry.
Sitrof provides premier consulting and technology solutions that enable life sciences companies to improve efficiency and mitigate risk.
We work from a unique position of experience and vendor neutrality to control and secure unstructured mission-critical information, ensure compliance, improve internal and external collaboration, streamline information sharing – and increase overall effectiveness in validated environments. Sitrof has helped six of the top 10 life sciences firms through the use of business analysis, workflow automation, topology mapping, document management and enterprise rights management.
Remember: The FDA and the EMA won’t go away. When an IT or content management need arises, you can trust Sitrof – a proven partner to Tier 1 and Tier 2 life sciences firms worldwide.
Sitrof has an exemplary record in regulatory affairs at Tier 1 and Tier 2 life sciences firms, managing millions of documents across disciplines, departments and external partners. LEARN MORE
Sitrof’s powerful pharmacovigilance solutions can help you reduce the time and cost of drug safety intake by automating the AE intake process – regardless of source or medium. LEARN MORE
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 QA process, improving overall performance, compliance and evaluation. LEARN MORE
Sitrof helps leading life sciences firms create order from chaos – streamlining information delivery, harmonizing processes and driving compliance, efficiency and profitability. Our vendor-agnostic approach allows us to effectively conquer any challenge on any system – FirstDoc, Documentum and more. LEARN MORE