Enterprises Solutions

Document Management System (DMS)

Karomi DMS provides the features and functions needed to securely and efficiently manage all regulated content and quality assurance related documents like Standard Operating Procedures, Methods, Work Instructions, and Specifications through the entire content lifecycle.

Karomi DMS is a fully 21 CFR Part 11 compliant document management solution designed specifically for the management of all regulated content as well as other documents your enterprise creates, consumes, and maintains.

It meets the DMS needs of LifeScience organizations like

  • Pharma (Brands, Generics, CMO)
  • Biotech
  • Medical Devices

It includes out-of-the-box functionality like

  • Audit Trails
  • Version Control
  • Electronic Signatures
  • Role based Security
  • Meta-data management
  • Central Repository
  • Indexing and Search
  • Change Control Workflows
  • Messaging and Alerts
  • Reporting and Metrics

The use of electronic document management has been proved to increase efficiency and aid regulatory compliance. Working electronically allows information to be shared, avoids duplication and reduces costs.

Overview
Connects
Contact
USA:   +1 (609) 436 9249

India:   +91 44 28345314-17

Sales :   sales@karomi.com

Support :   support@karomi.com

Partner:   partner@karomi.com