Global Business Process Harmonization
We harmonize your manufacturing and laboratory processes across all sites.
Enhance efficiency, compliance, and data integrity – building a foundation for global core systems and lasting digital excellence.
Simplifying complex processes and ensuring compliance
In pharmaceutical or laboratory environments, complex processes require efficient coordination, system integration and documentation. Global process harmonization serves to align and radically simplify processes across locations so that core systems can be rolled out and standardized interfaces implemented. This leads to a seamless integration of MES and LIMS, as well as ensuring integrated data management and storage.
msg industry advisors are at your side to support you in harmonizing your business processes and fully exploiting their performance through the integration of an MES and LIMS.
Global process harmonization for efficient IT system integration
Process harmonization is crucial when implementing pharmaceutical IT systems to meet the challenges in the pharmaceutical industry such as digitalization, new products (single dose/personalized healthcare (PHC)) and global growth. IT platform programs, such as the implementation of a global SAP system, create a company-wide interface to other production, laboratory, and quality systems. This also requires the introduction of globally harmonized systems in these areas. Local, location-specific systems are being replaced by global core systems, posing considerable challenges for individual locations. Global process harmonization aligns processes across locations and radically simplifies them so that core systems can be rolled out and standardized interfaces implemented.
Success Story Global Process Harmonization
Global Process Harmonization for Future-Ready Manufacturing
How a global pharmaceutical company standardized MES-driven processes to boost efficiency and to create a future-ready digital manufacturing environment.
Success Story MES Validation
GxP-Proof MES Harmonization
Creating a new MES landscape for a research-based pharmaceutical and biotech company.
Our Capabilities
msg industry advisors harmonize your production and laboratory processes across all production areas and locations creating the basis for your IT core and platform systems.
We get to know your individual environment on-site to identify pain points and potential for improvement – the basis for customized MES or LIMS solutions.
All systems connected to the MES or LIMS are visualized. Our BPMN 2.0 process modeling ensures a clear presentation and understanding of your processes for the future.
We create “position papers”, which document the harmonized processes and cross-location decisions, serving as a central reference framework for uniform implementation.
We create “position papers”, which document the harmonized processes and cross-location decisions, serving as a central reference framework for uniform implementation.
We implement solid data governance structures, which ensure the integrity and security of your sensitive data in compliance with data protection regulations.
By incorporating a QMS, we ensure that quality check processes are seamlessly integrated into manufacturing processes and product quality and compliance are guaranteed.
Even as requirements change, we ensure that your processes are permanently harmonized and efficient and comply with legal requirements.
Harmonizing production and laboratory processes together
Find out how you can take your production to a new level of operational excellence.