If you still use paper anywhere in your manufacturing process, you need to take a look at MasterControl Manufacturing Excellence™. Paper and human errors can cause unplanned downtime and preventable deviations. Not to mention the data integrity issues that come with paper. Considering the fact that the vast majority of FDA warning letters are due to data integrity, that isn’t a problem you can afford to have. By giving your employees the right tools, you can eliminate human error, decrease deviations and get your product released much faster.
Is Technology Enhancing the People on Your Factory Floor or Replacing Them?
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Manufacturing Excellence™: ROI Overview
As pressure mounts for manufacturers to find new ways to drive efficiency, reduce costs, improve quality and increase production – digitisation initiatives are a top priority.
17:07Episode 10: Future Proofing – Digital Production Records, QMS and Validation
Presented by MasterControl in collaboration with MedTech Association and MassMEDIC. In Episode 10 of this 10-part series, SVP of Strategic Growth Brian Curran and Principal Product Management Director
20:08Episode 9: Future Proofing – Continuing Production Beyond Exemption
Presented by MasterControl in collaboration with MedTech Association and MassMEDIC. In Episode 9 of this 10-part series, Senior Director Public Relations and Content Jennifer Hurst and Principal Produ
1:04:48Manufacturing Technology: Features and Functionality for Changing Environments
COVID-19 has exposed issues within the manufacturing industry, which may never be the same. The global pandemic illustrates why it is critical for manufacturers to be adaptable. Forward-thinking compa
23:02Episode 8: Documentation – Quality Event Management and Audit
Presented by MasterControl in collaboration with MedTech Association and MassMEDIC. In Episode 8 of this 10-part series, Product Manager Kim Jackson and Principal Product Management Director Terrance
18:03Episode 6: Documentation – Standard Operating Procedures (SOPs) and Work Instructions
Presented by MasterControl in collaboration with MedTech Association and MassMEDIC. In Episode 6 of this 10-part series, Product Manager Katie Farley and Principal Product Management Director Terrance
2:41MasterControl Manufacturing Excellence - APAC
Introducing MasterControl Manufacturing Excellence, now available in Asia Pacific. Experience a truly digital paperless, errorless and frictionless manufacturing experience. Read more here: https://ww
1:27MasterControl Manufacturing Excellence: Configuring Production Records With Ease
MasterControl Manufacturing Excellence™ is completely customizable, allowing users to easily build and edit their own production records.
1:37MasterControl Manufacturing Excellence: What Was the Inspiration for It?
SVP of Strategic Growth Brian Curran explains the motivation behind MasterControl Manufacturing Excellence™ and some of the history behind how it was developed.
Episode 5: FDA Current Guidance and Exemptions
In Episode 5 of this 10-part series, Product Owner Manager Dave Latimer and Principal Product Management Director Terrance Holbrook talk specifically about how digitizing helps with the complexity of
Episode 4: ISO vs. cGMP vs. FDA Requirements.
In Episode 4 of this 10-part series, Product Owner Manager Dave Latimer and Principal Product Management Director Terrance Holbrook discuss FDA requirements and how to comply with them.
Episode 3: Achieving and Maintaining an Audit-Ready State
Presented by MasterControl in collaboration with MedTech Association and MassMEDIC. In Episode 3 of this 10-part series, Validation Product Manager Erin Wright and Principal Product Management...
1:30MasterControl Manufacturing Excellence: Delivering Strategic Insights Into Manufacturing
MasterControl Manufacturing Excellence™ is one component in our platform. Companies can use multiple solutions to consolidate their data and gain insights into how to improve their processes.
17:22Episode 4: ISO vs. cGMP vs. FDA Requirements
In Episode 4 of this 10-part series, Product Owner Manager Dave Latimer and Principal Product Management Director Terrance Holbrook discuss FDA requirements and how to comply with them. Key takeaways
Episode 2: Elevate Your Quality Management System
In Episode 2 of this 10-part series, SVP of Strategic Growth Brian Curran and Principal Product Management Director Terrance Holbrook discuss the cost benefits of a QMS.
Episode 1: An Introduction to Quality Management System (QMS) for Regulated Industry – Next Steps
In Episode 1 of this 10-part series, Vice President of Product Rajesh Talpade and Principal Product Management Director Terrance Holbrook explain the basic ins and outs of optimizing a QMS.
