ROS has conducted a global assessment to identify available software supporting different regulatory, quality and safety functions. Overall, ROS has identified 88 software from respective functions such as,
1. eCTD Publishing
2. Document Management (DMS)
3. Trial Master Files (TMF)
4. Labelling Management
5. Artwork Workflow Management (AWM)
6. Quality Management software (QMS)
7. Pharmacovigilance software (Pv)
8. Regulatory Information Management software (RIMS)
The following graph represents number of software available for each function outlined above.
Select functions of your interest from the list above to explore the list of software available and their summaries.
For complete report of software, companies providing those software, broad features, their locations and clientele, please download the complete report here.