MES Service Factory
We are dedicated to improving and testing your Manufacturing Execution Systems (MES) with unparalleled precision and efficiency – through services tailored to the dynamic needs of modern pharmaceutical companies.
Standardizing test and verification activities
In the pharmaceutical industry, system reliability is not negotiable. Through structured standardization and optimization of your MES recipe design and testing activities, the number of errors can be significantly reduced, operational efficiency increased, and production schedules made more predictable. A reduction in operating peaks can also be achieved and a seamless process is guaranteed. However, for solutions to be successfully rolled out as standards, they must meet your specific requirements.
msg industry advisors combine MES expertise with a comprehensive understanding of pharmaceutical processes and compliance requirements and offer innovative and compliant solutions with the MES Service Factory.
Design, test and verify master batch records
The Master Batch Record (MBR) forms the backbone of pharmaceutical production. As specialists in this field, we design, test, and verify MBRs that meet the highest industry standards and are optimized for efficiency. Thorough testing and verification ensure that each MBR is perfectly aligned with your operational and regulatory requirements. This ensures that your manufacturing processes are seamless and error-free, and that product quality remains consistently at the highest level. We support you effectively in critical, labor-intensive phases and act as a strategic partner, covering standardized activities and freeing up your resources.
Increasing efficiency and reducing costs together
We offer a proven, standardized approach. If this does not fully meet your individual requirements, we adapt it to suit you. When designing our offer, our focus is on maximum flexibility – by adapting to your operational peaks and troughs, we support you exactly where you need us.
Our services include:
MES system audit:
Validation tests in the form of test management:
Test of release updates & bugfixes:
MBR design:
MBR verification:
Relief during updates:
We redefine standardization and bring order to the dynamic
pharmaceutical landscape. Improve your MES precision and efficiency with us.
Further expertise in Manufacturing & Laboratory Excellence
Digitalization Strategy
Our digitalization strategy seamlessly integrates physical and digital aspects and ensures quality, efficiency, and sustainable competitiveness.
Global Business Process Harmonization
In pharmaceutical production, the synergy of business process harmonization and system implementation is crucial.
Requirement Engineering & Vendor Selection
Careful analysis and vendor selection are required to select and implement the right IT system for your requirements.
System Implementation & Integration
For the successful implementation and integration of MES and LIMS, it is important to keep optimized production processes and the highest quality and compliance in focus.
