System Implementation & Integration
We seamlessly implement and integrate MES and LIMS solutions into your system landscape.
Ensure compliance, enhance efficiency, and build a strong foundation for connected, future-ready manufacturing processes.
MES and LIMS as the key to compliance, efficiency, and quality
The demands placed on pharmaceutical companies in the area of production processes are many and varied. In addition to increasing effectiveness and productivity, numerous quality standards and regulations need to be taken into account. The implementation and integration of Manufacturing Execution Systems (MES) and Laboratory Information Management Systems (LIMS) help ensure compliance, optimize production processes, guarantee globally consistent procedures, and achieve innovation benefits. MES and LIMS also offer security, traceability and enable the use of modern technologies to cope with constant change. If the system implementation is to be successful in the long term, the focus must be on integration into your existing process and system landscape. This is how we ensure cooperation between the business side and IT.
As industry experts, msg industry advisors understand the production processes of the pharmaceutical industry. In combination with our knowledge of various MES and LIMS vendors and all the necessary guidelines, we make your implementation project a success.
Overcoming implementation and integration challenges together
There can be many reasons for implementing a system: The first step from paper documentation into digitalization, an elementary software upgrade, the migration from one system to another or a holistic solution across multiple locations. To ensure a seamless transition, we support you through the entire process with industry and process expertise and involve all relevant departments and stakeholders in a targeted manner through appropriate communication.
Our Capabilities
msg industry advisors are your trusted partners for the implementation and integration of MES and LIMS with a comprehensive range of services – regardless of vendor or system.
Our standard process model for the pharmaceutical industry is independent of vendors and systems and can be specifically adapted to your processes. This enables us to support your project with maximum flexibility.
We accompany the entire system implementation process – from your individual starting point with existing operational processes to the complete implementation of your objectives.
During the entire implementation process, we ensure compliance and quality (e.g., GAMP 5.2, ISA95, 21 CFR Part 11, EU GMP Annex 11, VDI5600).
Based on our established standard process model and automation standards, we seamlessly integrate your systems vertically and horizontally to create a holistic, systematic IT architecture.
On request, we can take over the project management of your system implementation, including organization, planning and communication.
In addition to technical expertise, the human factor is crucial to the success of your project. We support or take over your change management through targeted stakeholder communication, taking into account the various interests and priorities.
Successfully introducing and integrating MES and LIMS
Are you facing the challenge of an MES or LIMS project? We support you in all your needs.