Milestone Consult offers a wide range of MES services. The following are the most important services that are successfully used by pharmaceutical companies.
Milestone Consult sees the possibility to optimally control and document computerised machines and processes in MES (manufacturing execution systems) in order to ensure the quality and profitability of the products. Through these complex and integrative MES issues, our consultants have gained important experience in many projects, which we would like to contribute to your project.
We support you in the analysis, creation and verification of your MES relevant processes.
We support you in designing a suitable test
strategy for your project and implement it.
We support you in the planning and implementation of your complex MES projects.
We support you in the design, recording and maintenance of your MES master data.
We support you in all topics related to your MES migration.
We support you in developing a rights and roles concept tailored to your MES and your user roles.
For an international pharmaceutical company, we have designed MES production recipes and implemented MBR verification to ensure the quality of recipes for production.
For an international pharmaceutical company, we have carried out the implementation of user acceptance tests (UAT) and interface testing (SAT) as well as verification of master batch records (MBRs) after MES migration for the qualification of the MES system for the production of an active substance with a biotechnological process.
For an international pharmaceutical company with one of the locations in Vienna, we perform the MBR verification and checks for MBR changes and new implementations.
For an international pharmaceutical company with one of the locations in Vienna, we perform training for the MES system PAS X, including preparation of test data and setup of the training environment. Additionally, we will support you in the design and testing of rights holder profiles.
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