In order to aid and help QA teams of manufacturing concerns and laboratories, SCC has integrated Quality Management Systetm (QMS)/Corrective and Preventive Action (CAPA) Management module that will help in managing Out of Specification products identified by lab process. QMS/Capa module will have following major features in addition to reports and views.
1. Upload all the QMS documents (process/guidelines or checklist) in the application that act as a single point reference for all lab staff
2. Checkout of documents and checkin of new version keep automatically all versions of QMS documents
3. Associate departments with the documents thus can automatically trigger training need of staff everytime a document is changed
4. Keep an log of all training and scores of the staff
5. Logging all Non-Conforming results or issues in incident register
6. Corrective and preventive action will be logged and tracked to closure
In addition to OOS, the module will allow incident to be created by the users that may be relating to periodic Audit observation, Non conformance identified by internal or external auditors, any adhoc preventive identification of likely problem.
The module will help lab staff and quality assurance team in its initiative to assure quality but also help in getting ISO/Regulatory certifications related to their products and offering.
The blog will be open to take ideas/suggestions from community seeking new features or comments on features required. SCC welcome suggestion on expected features and functionality from the prospects and interested community.
