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Execute Effective Manufacturing with the Syncade MES

Execute Effective Manufacturing with the Syncade MES

The Syncade MES improves manufacturing operation to drive your production goals. Whether it is compliance regulations, excessive work in process, or inefficient use of resources, increasing production costs cut into your profits. The Syncade MES combines document, equipment, and materials management into electronic work procedures to create an optimized manufacturing environment for Cell & Gene Therapy companies.

NECI Can Help With:

Equipment Logbook
Tracking equipment usage, status, and maintenance helps to ensure efficient, predictable lab performance. This is an important part of modern, paperless operation in line with digital transformation and Pharma 4.0 initiatives.
Material Tracking
Tracking the usage of raw materials as well as the in-process flow of materials allows the early clinical lab to operate efficiently and establish the foundation of paperless processing and tracking needed as clinical production becomes necessary.
Electronic Batch Record
Building your processes into Electronic Batch Records ensures operators deliver in line with your process requirements, making every operator your best operator.
Dynamic/Advanced Scheduling
By collecting data from across the organization, our Real-Time Modeling System can consolidate, analyze, and present an accurate model of the entire process. The model then produces an optimal scheduling overview with debottlenecking and capacity analyses for process optimization.
Document Management
Cell & Gene Therapy companies benefit from electronic document management systems that help to reduce paper and make information more accessible and reliable.
Training Records Management
Ensuring that lab personnel have the correct training and certification to maintain consistent operations and sets the stage for more rigorous learning management. Keep critical research moving by utilizing a virtual training environment without taking time in the lab.
Process Knowledge Management
Seamlessly manage product and process specifications throughout the drug development lifecycle with our PKM software, Fluxa. Inherently designed to facilitate collaboration, it enables global sites, functions, CDOs, CMOs, and CDMOs, to work together to scale recipes and execute technology transfers.
Contact us to learn more about the products, services, and solutions that NECI provides to Cell & Gene Therapy organizations.