Increase Clinical Trial Team Productivity
Eliminate manual paper handling tasks by automating the acquisition, classification, indexing and archiving of documents, email and medical images
Save time and money and enhance quality by acquiring documents at the point of creation. Capture regulatory agency compliant digital signatures.
Ensure document quality, track regulatory document compliance and lower auditing costs
Freedom for your clinical trial workforce with support for Windows® PCs and Apple® Mac OS. Securely access records online or offline.
Supports standards-based technologies to facilitate interoperability with existing systems. Open architecture.
Share content securely online or offline using US FDA, EMEA and HIPAA compliant FIPS-140 encryption standards.
SureTrial® eTMF is a regulatory document solution which enables BioPharma clinical trial stakeholders to securely acquire, view, share and manage clinical trial electronic documents and medical images for electronic trial master files. SureTrial maximizes productivity and document quality for clinical trials by automating manual paper-handling processes such as document signing, classification, indexing, archiving and other labor intensive clinical trial content management processes. SureTrial ensures that study documents, medical images and eRecords for BioPharma clinical trials are always available to all stakeholders, either online or offline. Using industry standard technologies, SureTrial eTMF lets you create an interoperable eTMF model with published templates, or 'content classification models.' SureTrial lets you use any eTMF content model, or you can modify and edit provided content model templates to meet your needs. SureTrial is used by clinical trial Sponsors, Investigators, Clinical Research Associates and others who wish to install automated, secure, and cost-effective eRecord handling in clinical trials.
Eliminate paper at the point of creation - deploy SureTrial® eTMF cloud edition for clinical trials.Learn More
SureTrial® eTMF is a regulatory document solution which enables BioPharma clinical trial stakeholders to securely acquire, view, share and manage clinical trial electronic documents and medical images for electronic trial master files. Click on the video above for more information.Continue reading
Create, edit and deploy interoperable content classification models
Easily import, edit or create health science content classification models using a simple to use graphical user interface. Supports published health science vocabularies and open Enterprise Content Management systems
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