Life sciences

Document Locator gives companies in life sciences, including pharmaceuticals, biomedicals, and medical device manufacturers, the document control tools necessary to manage regulated content through each step in the development process, from discovery to delivery. It provides the foundation to improve quality and collaboration, and meet FDA regulatory compliance.

With Document Locator you can automate reviews and approvals – and capture an audit trail of every event for regulatory and quality overview. Integrated records management allows you to accurately capture, identify, store, and dispose of records properly.

Automate the build-out of folder structures according the TMF Reference Model (Trial Master File Reference Model). The entire TMF Reference Model is a set of instructions on how to arrange a large hierarchical tree and folder structure, with all of the information laid out clearly. It provides a standardized taxonomy and metadata. Much of the structure and properties needed to manage files in accordance with eTMF can be automated in Document Locator.

Be ready for eCTD submissions. Document Locator sets the framework for capturing the required information in an organized environment necessary for future eCTD submissions.