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The ability to adapt to change is critical when running a clinical trial. So you should expect the same from your eClinical partner. You need a platform that offers a balance between powerful technology and expert professional services, like TMF document processing, migration, and system validation. Flexibility and scalability should be at your fingertips for both the technology and human touch required to handle your study with care.
A practical, secure, compliant single access point for TMF documentation, supporting all essential document processes and reducing the time, costs, and risks of TMF management. Connected, fluid document collaboration and learning management system solutions ensure a complete approach to clinical documentation and compliance.
Millions of Documents Processed and Counting
Successful FDA, EMA, MHRA, PMDA, and GCP Inspections
40+ TMFs Rescued Mid-Study
Managed Single TMFs with over a Million Documents
Over 75% Risk Reduction
Thousands of Active TMF/eTMFs
TMF Reference Model Committee Members and Influencers
12 Years of TMF Leadership
