COLLABORATE is the newest regulatory technology solution from GlobalSubmit. Designed specifically to meet the needs of life science regulatory professionals, our eDMS is user friendly, meets regulatory compliance standards (ICH, 21 CFR Part 11) and is available via a cloud-based deployment.
We invite you to register for a first look at COLLABORATE. The Tuesday, June 21st webinar will give an over of GlobalSubmit’s document management system functionality and user benefits.
- Affordable for small to mid-sized life sciences company that needs a system compliant with industry regulations
- Domain specific, cloud-based system provides secure and global access
- Integration with Microsoft’s Online Office suite is unique in the industry and makes company integration seamless
- Built-in eCTD authoring templates for quick, high-quality document creation
- Simple, single click for more effective user adoption
- Validated environment and automated 21 CFR compliance requires no additional steps
- Device agnostic for global site and diverse platforms
- Simplified workflows with automated task management and notifications