A Life Science Article from MasterControl
A life science article from MasterControl focuses on quality process management (i.e. an integration of document control, CAPA, change control, audit management, etc.) and on complete regulatory compliance (FDA, ISO, CLIA, etc.)
How does it work?
The MasterControl Documents solution acts as the fulcrum for all MasterControl solutions. It allows life science companies to save time by automating and centralizing the creation, routing and approval of documents and by ensuring document version control, document tracking, records management and complete regulatory compliance. MasterControl Documents can also be complemented by additional quality management solutions which include the following:
- MasterControl Customer Complaints
- MasterControl CAPA
- MasterControl Change Control
- MasterControl Training
- MasterControl Forms
- MasterControl Audit
- MasterControl Electronic Submissions
When you read a MasterControl life science article, you'll probably want to give electronic quality management a try (if you haven't already). Once you do, the FDA's CFR 21 Part 11 regulation specifies that validation of the electronic system (or the software) must take place. MasterControl provides validation services as well as implementation, training and technical support.
Contact MasterControl for more information regarding quality control processes.