Document Management
An organized repository of documents, images and associated content, TMFPro serves the complete needs of a Trial Master File of any clinical study, as demanded by domestic and international regulatory agencies. The Trial Master File should not be complicated, but it must manage all study documentation efficiently and give access to all those who need it, with ease.
TMFPro meets the needs of paperless study document and content management in accordance with international and local regulations, as follows:
- ICH GCP compliance
- Secure electrionic document storage
- Electronic signatures
- Quick response to regulatory audits and inspections
- Easy upload and reporting
- Quick set-up and new program additions
Learn how TMFPro can organize your study documents, while complying with regulatory agencies
