Dietary supplement manufacturers have to follow the guidance in 21 CFR Part 111. Success depends on having quality processes that integrate with every stage of the product life cycle.
The MasterControl Product Lifecycle Excellence Platform brings together product development, manufacturing, quality and postmarket activities. It automates processes to improve efficiencies and ensure compliance.
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The good manufacturing practices (GMP) regulation for dietary supplements, 21 CFR Part 111, requires proper controls for manufacturing, packaging, labeling and holding operations. They also require that those controls are properly documented. MasterControl solutions bring automation to the process, which ensures compliance and improves quality.
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.