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Manufacturing
Manufacturing
MES Software Solution
MES for Medical Devices
Tired of rigid, clunky systems that slow down your medical device manufacturing processes? Now you can get the flexibility, configurability, and scalability traditional manufacturing execution systems (MES) have been missing with MasterControl Manufacturing Excellence.
Legacy systems struggle to adapt to today’s medical device manufacturing demands. With innovative manufacturing execution software like MasterControlManufacturing Excellence, your company can achieve a truly paperless, errorless, and frictionless production environment.The software solution’s digital production records offer limitless flexibility and make it easy for medical device manufacturers to automate, optimize, and adapt their existing processes.
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FAQs about MES for Medical Devices
What are the specific benefits of implementing an MES for medical device manufacturing?
Configurability is a key benefit of a purpose-built MES for medical device companies. Unlike traditional, inflexible manufacturing execution software, MasterControl’smodern MES lets you quickly scale down for small batches or scale up to increase production capacity. Other advantages include easily adaptable processes and greater flexibility and accuracy in managing production records.
How does an MES help with compliance and regulatory requirements in the medical device industry?
Regulators demand proper documentation and access to audit-ready information. MasterControl’s innovative MES for medical device companies provides real-time access to up-to-date digital records so you can demonstrate continual compliance. With all your data digitized and connected within a modern MES software solution, compliance has never been this easy.
Are there any industry-specific standards or certifications that an MES should adhere to in the medical device field?
ISA-95 and DIN EN 62264 are prominent standards used to define MES solutions. In the medical device industry, the effectiveness and value of an MES is determined by its ability to help organizations adhere to current good manufacturing practices (cGMP) and quality guidelines set forth by agencies that regulate medical device manufacturing.
How does an MES improve traceability and quality control in the production of medical devices?
A modern MES for medical device companies boosts real-time visibility. With the fully connected digital records provided by powerful MES solutions like MasterControl’s Manufacturing Excellence, medtech companies can eliminate the siloedproduction systems and manual process inefficiencies that often cause barriers to product quality and traceability.
Resources on MES for Medical Device Manufacturing
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Benefits of a Modern MES for Medical Device Manufacturers
Conventional manufacturing execution software is inflexible, inefficient, and disconnected from other vital processes. Below are some examples of the many ways innovative tools are revolutionizing medical device manufacturing.
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Fully digitized device history records.
If you’re using paper anywhere along the line in your medical device manufacturing processes, you’re leaving the door open for human errors and data integrity issues. Robust manufacturing execution software with built-in electronic device history records (eDHR) eliminates data entry errors, automates data integrity checks, and enables device manufacturers to proactively track production data that has the potential to impact quality.
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Unmatched review-by-exception functionality.
By the time you’ve identified and corrected an issue using your legacy MES, the entire production process has already been slowed down or ground to a halt. MasterControl’s MES for medical device eliminates line-by-line reviews at the end of production, allowing you to fix errors in real time and easily identify and address the issues that create exceptions.
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Streamlined, error-proof device history record processes.
Every medical device manufacturer needs a system that captures device history data quickly and accurately and maintains it all in a centralized, accessible location. MasterControl manufacturing execution software includes eDHR capabilities that optimize production record processes and eliminate common mistakes and issues related to incomplete documentation.
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Simplified compliance.
It’s a monumental challenge for medical device manufacturers to keep pace with complex regulatory demands regarding design, documentation, supplier control, and other compliance-critical aspects of development and production. MasterControl’s MES for medical device automates processes, enhances efficiency, and accelerates development life cycles, all of which goes a long way to helping manufacturers maintain a continual state of regulatory compliance.
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Enhanced connectivity of data, processes, and people.
Visibility, communication, collaboration, and integration are critical elements you’ll need to succeed in medical device manufacturing. MasterControl manufacturing execution software seamlessly connects site operations, line performance, and quality teams to take connectivity to new heights and establish truly paperless production.
Learn more about MES for medical devices.
Accelerate and Automate Processes
Traditional MES tools don’t offer the flexibility modern manufacturers need. Discover how our modern manufacturingexecution software adapts to suit your processes and business requirements.
Establish End-to-End Control of DHRs
Find out how a complete eDHR system will enable you to capture and leverage all the data you need to meet regulatory requirements and improve production and quality.
See the Latest Digital Manufacturing Research
Many medtech manufacturers are lagging in digital maturity, but this report shows how leaders are gaining an edge by implementing manufacturing execution software.
Talk to an Expert
MasterControl specialists are on hand to answer your questions about manufacturing execution software and help you find the best fit for your medical device company.
