Evaluating a SaaS-regulated CSP for clinical research can be complex. Our comprehensive checklist provides a clear, structured framework to help you confidently assess vendors and select a solution that ensures regulatory compliance, operational efficiency, and scalability.

This essential resource helps you evaluate CSP capabilities, including:

⚖️ Regulatory Compliance: Built-in adherence to FDA 21 CFR Part 11, GDPR, HIPAA, and ISO 13485 standards.

📜 Security and Document Management: Robust encryption, audit trails, automated workflows, and advanced search functionalities.

🌐 Integration and Scalability: API support, seamless third-party tool integration, and scalability for global trials.

✅ Vendor Evaluation: ROI transparency, cost-effectiveness, and proven vendor expertise to support your team.