Dietary supplements manufacturers follow strict quality guidelines amongst increasing regulatory oversight. Instituting quality processes from R&D through manufacturing and commercialization is imperative to be successful.
The MasterControl product lifecycle excellence platform is designed to help dietary supplement manufacturers automate paper-based quality management and manufacturing production record processes to improve efficiencies and ensure compliance.
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The U.S. Food and Drug Association’s (FDA) Good Manufacturing Practice (CGMP) regulation, 21 CFR Part 111, requires that the proper controls be in place for dietary supplements during manufacturing, packaging, labeling, and holding operations. The MasterControl Product Lifecycle Excellence solutions helps dietary supplement companies leverage quality and compliance requirements by automating and accelerating quality processes across the enterprise - all on the MasterControl Platform™.
With an integrated quality management system (QMS) that crosses the traditional barriers between quality and manufacturing, you can improve efficiencies and increase product quality across the company. MasterControl’s platform connects processes like document control, training management, corrective actions, along with batch, device history, calibration and maintenance records throughout your product lifecycle.
MasterControl allows users to access information and perform tasks using a tablet or a smartphone. Mobile access offers greater flexibility for users and helps boost overall efficiency and productivity.
Leveraging cloud technologies is critical for automating quality processes. Companies without access to its speed and adaptability will struggle to maintain a competitive edge. MasterControl isn't just a cloud-based solution. It’s dedicated teams and specialized tools to help make your implementation simple and your experience seamless.
MasterControl provides an effective framework for a company's quality management system (QMS) by automating all documents- and forms-based processes, connecting all quality processes, and providing a centralized location and single source of truth for all documents and data.