Manufacturing - Quality - Solutions
A manufacturing execution system is key to efficient and compliant pharmaceutical manufacturing. Despite how complex this industry can be, the MES solution you choose doesn’t have to be overly complex. An integrated software solution can connect your manufacturing activities with the right people at the right time. Find out how MasterControl’s modern MES solution can help you complete essential manufacturing tasks including:
Going digital means you can overcome common manufacturing execution system challenges. Connecting every segment of a manufacturer’s value chain is essential to create new levels of transparency and adaptability for modern laboratories and shop floors.
Manual data collection introduces a variety of errors, data integrity risks, and performance inefficiencies. Automated processes will not allow incorrect, missing, or out-of-date entries. Digitizing production records creates productive connections between people, processes, and systems, which significantly reduces production errors.
Many manufacturers don’t have in-process visibility into all that data. Much of it is unstructured and tucked away in filing cabinets or storage boxes. Using modernized data management tools, you can analyze complex data sets in a fraction of the time it would take using manual processes.
Manufacturers who continue to use pen and paper or spreadsheets to track vital steps risk being unable to manage successful production as well as deviations and corrective/preventive actions. Missing or damaged records can seriously impact lead time and lead to delayed releases. This is too late for effective quality control and may require returning and repeating earlier steps. A digital MES for pharmaceutical manufacturing with electronic batch records is key to overcoming inefficiencies and delays in manufacturing.
Manual manufacturing execution systems fail to efficiently monitor and connect production tasks. A modern pharma MES can establish work-in-progress visibility as well as real-time collaboration and data sharing across all business units. This makes real-time line adjustments possible to minimize misallocations, rework, and waste/scrap.
One of the most common causes of delays in batch releases is related to the quality function - specifically, missing batch information. The review and clarification processes are cumbersome as they involve several reviews by different staff members, which forces organizations to increase their quality control efforts and expenditures to identify and locate errors. This is non-productive time. The real-time review by exception approach eliminates line-by-line reviews at the end of production. This dramatically reduces lead times and accelerates product releases.
For most production environments, a traditional MES is too expensive, complex, and rigid to implement. We have something better.
Ensuring the quality of your manufacturing products and processes is paramount – and possible with the right pharma MES.
When you need to demonstrate compliance, accountability, and performance – real-time access to electronic manufacturing records is key.
Find the perfect MES for your pharma manufacturing needs. Discuss solutions with a personal representative.
Our goal is to help you succeed in your manufacturing operations. You’ve got questions about pharma MES solutions. We’ve got answers and we know they’ll make your work burdens lighter.