AQ E-ISF & PSF
Go Digital with AQ’s investigator site file solution designed to reduce administration, improve speed and compliance for sites and clinical trials teams.
The AQ eISF and PSF is designed with clinical trial personnel at the heart, enabling collaboration around your studies, eliminating inefficiencies associated with traditional paper based systems and removing uncertainty and confusion.
The AQ ISFs have all the features required but without the high costs.
Experience Collaboration
- Multiple user access: Allows multiple users to access the repository and collaborate on the same data.
- Cloud-based solution: Provides accessibility from anywhere with an internet connection.
- Team collaboration: Invites teams to collaborate and share data.
- External collaboration: Allows collaboration with external governing bodies such as CRAs from sponsors.
- Customizable time limits: Gives the ability to set custom time limits for data access.
- Commenting and updates: Allows collaborators to add comments and updates directly from the repository.
- Centralised communication: Centralizes all communications in one place, reducing confusion and improving efficiency.
Automate compliance and engage with workflows
- Reduce regulatory compliance risks by organised, tracked and auditable documents straight from your browser.
- Send workflow notifications to collaborators when critical steps completed
- Be part of workflow process and never miss an assigned action
Engage with Live Documents
- Central repository: Creates a central repository with folders for all sites and trials, providing enhanced role-based access.
- Document upload: Document upload: Allows for the upload of key documents to folders with unlimited storage and security.
- Document management system: Acts as a general document management system, reducing the reliance on paper-based documents.
- Improved organisation: Enhances organisation and accessibility of important documents.
- Increased security: Increases the security of sensitive documents with enhanced access controls
Control document lifecycle and versioning
- Real-time inspection readiness: Our eisf clinical trials ensures the latest version of a document is always available and ready for inspection.
- Document locking: Our electronic investigator site file Locks approved documents with added version control, reducing the risk of changes being made to finalised documents.
- Document archiving: Archives all documents, providing the ability to retrieve them when necessary.
- Document elimination: Eliminates redundant and duplicate documents, reducing clutter and improving organisation.
- Version control: Tracks changes made to documents and provides a clear history of document modifications.
Access and control at your fingertips
- Enhanced compliance with 21 CFR Part 11 for secure electronic record keeping .
- Integration with global regulatory requirements for archiving and eTMF for streamlined compliance.
- Flexible role-based access control for customising user access to folders and clinical trial regulatory documents
- Advanced auditing capabilities, including the ability to view and download detailed audit logs for increased transparency and accountabiliy.
