Clinical
Current Good Laboratory Practices (cGLP)
Companies within the stringently regulated FDA environment know how vital compliance to implement current good laboratory practices is to their success. The guidelines set forth by GLP help regulated companies meet FDA requirements as they develop, manufacture, and distribute their products.
The MasterControl Suite and cGLP
For compliance to standards of current good laboratory practices, the FDA continues to require all core processes and systems within a company to be identified, evaluated, and prioritized. MasterControl's system evaluation allows companies to attain compliance, and all the following, from a trusted professional software company.
- Streamline Approval Cycles
- Automate Document Distribution
- Institute Company-Wide Quality
- Accelerate Testing Turnaround
- Manage Quality, Solve Problems
MasterControl Can Help Streamline Management of Current Good Laboratory Practices (cGLP)
MasterControl was the very first content and quality management system provider to offer software applications that directly address the challenges of complying with cGLP and other FDA regulations. Our software solutions include integrated, easy-to-use applications that help companies automate the requirements of GLP compliance, such as GLP audit, GLP training, and other requirements.
Our quality management software for cGLP includes the following:
- Document Control/ Document Management
- Corrective Action, Preventive Action (CAPA)
- cGLP Change Control
- cGLP Training Management
- Deviation Management Software
- Audit Management
- Forms-Based Process Automation
- Electronic Submissions Readyness
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