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.
Our Capabilities
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 team tests your MES using a risk-based approach to ensure perfect functionality throughout the entire software lifecycle. If problems are identified, we initiate rework with the supplier or the system test approach.
We take on the planning, organization, and execution of validation tests, (OQ, PQ, UAT) as well as the associated documentation – from the creation of test plans, specifications and reports to the creation and tracking of the traceability matrix and the operation of test systems such as Jira or ALM.
We ensure that your systems are always compliant with technological advancements and legal requirements. Our proactive approach minimizes downtime and maximizes productivity.
Correct MBRs are crucial for seamless MES operation. We independently create the required MBRs and a complete overview of your recipe landscape – the basis for a holistic picture of your processes and optimization suggestions.
We verify your existing MBRs for logic, relationships, user-friendliness, and efficiency and perform official MBR tests for release. The result: A valid, efficient library and MBR landscape.
Updates also entail similar workload peaks as system implementations – we are happy to support you.
Increasing efficiency and reducing costs together
We redefine standardization and bring order to the dynamic pharmaceutical landscape. Improve your MES precision and efficiency with us.