Thank you.

To all those on the front lines, behind the scenes, and everywhere in between, MasterControl is proud to support all you’re doing to combat COVID-19.

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The platform for quality.

Explore how the MasterControl Platform™ digitizes, automates and connects quality and compliance across your entire product life cycle.

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Benefits of Using MasterControl

01

100% Decrease in Data Input Errors

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No, really.

When Wellington Foods implemented MasterControl’s Manufacturing Excellence solution, they saw a 100% decrease in common data input errors. No input errors means no wasted hours tracking down what went wrong, which leaves you more time to focus on what you do best.

02

92% Reduction in Quality Review Time

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Three hours? Try fifteen minutes.

Fully digital data input and automated workflow routing means a drastic reduction in the length of the quality review process. For Legacy Pharmaceutical Packaging, that means what used to take three hours per batch record can now be accomplished in only fifteen minutes.

03

30% Efficiency Boost

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Get more results for less work

Life sciences manufacturers that make the move to our digitized and automated system achieve efficiency gains of 30%. That means big savings on staffing and overall manufacturing costs and more time and money for you to focus on your innovation pipeline.

04

25% Reduction in Total Deviations

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Change your game.

MasterControl’s integrated digital production records and quality event analyzer provides a risk-based approach to assessing a deviation’s potential to turn into a CAPA, which allows you to dramatically reduce the impact of the deviations in your production environment.

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The Ultimate Guide to Digitizing the Shop Floor

Manual processes still dominate the shop floor, where people on the production line have been left to deal with paper, spreadsheets and other standalone systems to create, maintain, approve and release production records.

Trends Brief 2020

The Ultimate Guide to Connected Quality Data

Life sciences organizations are increasingly moving away from document-dependent quality management methodologies and toward a more data-centric model.

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FDA Fronts Pivotal Life Sciences Trend in 2020

In 2019, the U.S. Food and Drug Administration (FDA) introduced its Technology Modernization Action Plan (TMAP), a program designed to bring the organization up to speed with the latest technologies in order to expedite breakthrough discoveries with the intent of improving public health.