Current Good Laboratory Practices (cGLP)

Software for Ensuring Compliance to Standards for Current Good Laboratory Practices and Facilitates Management of 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.

Toolkit

Clinical Management Toolkit from MasterControl

Download

Product Videos

Hundreds of companies around the world use MasterControl to automate core business processes and document management activities to promote collaboration, improve decision making, and accelerate time to market.

Play

Demo Introduction: MasterControl Clinical Quality Management System

Play

Demo Introduction: MasterControl Clinical Audit Management System

Play

Demo Introduction: MasterControl Clinical Supplier Management Software

Play

Demo Introduction: MasterControl Clinical eTMF Management System

Free Resources

Select all the resources you’re interested in downloading

White Paper: 8 Best Practices for Compliant and Quick Software Validation in the Cloud White Paper: Quality Audit - A Tool for Continuous Improvement and Compliance White Paper: The Top 5 Benefits of Electronic GLP Audit Management White Paper: Managing CLIA Compliance Costs: 6 Mistakes Every Laboratory Should Avoid
Product Data Sheet: MasterControl GLP Studies™ Product Data Sheet: MasterControl GCP Studies™
Toolkit: Clinical Management Toolkit from MasterControl

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 ensures that all standards to assure cGLP are met and sustained in hundreds of FDA-regulated companies worldwide.

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

For More Information on Current Good Laboratory Practices (cGLP)

For more information about standards for current good laboratory practices (cGLP) or software for ensuring compliance to Good Laboratory Practice (GLP), please feel free to contact a MasterControl representative.

The QMS Provider for the FDA

MasterControl Inc. and its partner, i4DM, are expanding their FDA project, serving as the QMS providers for a second FDA division. The two companies have been the QMS providers for the FDA's Office of Regulatory Affairs since 2009. Now they will also serve as quality providers for the Division of Pharmaceutical Analysis, which is part of the FDA's Center for Drug Evaluation and Research.

Learn More