Manage clinical trial data effectively with customizable and accessible clinical document management solutions.
Security, transparency and accessibility are key factors when considering the management of clinical trial documents.
Continuous oversight
We offer Veeva Vault as part of our clinical research services. This robust electronic Trial Master File (eTMF) system effectively manages all your clinical trial documents, allowing modifications and configurations while maintaining strict security and access control. This user-friendly system gives you continuous oversight of contract research organization delegated tasks.
Our eTMF services for Veeva Vault guarantee real-time inspection readiness, user-friendly filing and easy 24-hour access to all approved documents. The integration with the Veeva Vault Clinical Trial Management System (CTMS) into the Vault Clinical platform results in improved efficiency.
Designed for small biotechnology and pharmaceutical companies, our unique stand-alone service gives you experience of the eTMF system of Veeva Vault while our document management team can develop a tailored solution that matches your requirements.
Services include:
- Tailored client eTMF system setup
- Study specific eTMF setup
- End-user training
- Client eTMF management
Why choose eTMF services from SGS?
We are recognized as the benchmark for quality and integrity in clinical trial data management. We have the experience and expertise to ensure your clinical trial data is secure and assessable at all times.
