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Our customer support team is your contact partners for all support and service requests. The qualified employees at our service centers are always available to you on request. Professional expertise and short reaction times are guaranteed.
Our customer service centers are the central contact points for all of our customers’ service requests. Our self-service portal is also available to all our customers. It offers direct access to the information and solutions they need.
Our project teams offer remote support for successfully implementing and driving forward your MES project. If required, we can also provide personal support on site, e.g. with the management, configuration, and parametrization of your Werum PAS-X system. This gives you the space to concentrate on other tasks.
Incident and problem management is provided on the basis of the contractually specified service level agreements with our customer services — up to 24 hours a day, 7 days a week, and 365 days a year.
Make use of our expert knowledge. We transmit our expertise to your employees by means of targeted training sessions and support during production. Their knowledge is deepened and production efficiency is increased.
We advise customers in the areas of medical devices, biotechnology, food, and cosmetics, and we support our pharmaceutical customers from the regulated industry in a wide range of different ways. Ask us.
Pursue value-based and innovative production IT strategies around Werum PAS-X MES driven by our Principal Consulting & Client Advisory services.
We make our committed consulting team available in order to ensure the fast and effective implementation of your PAS-X MES project. We provide you with the best possible advice on the PAS-X functionalities and the creation of MBRs thanks to our expert knowledge.
With PAS-X KPI/OEE we offer you a lean, independent software product for the real-time monitoring of production and packaging lines in order to boost production performance in your pharma and biotech plant.
Our consulting solutions include the creation of your specific business process descriptions on the basis of industry-specific best practices. You profit from standardized, harmonized, and optimized processes in your pharma and biotech plant.
Would you like to know how to successfully validate your processes, achieve regulatory filing and further improve the quality of your products? Use our process knowledge and statistical toolbox to gain deeper insights into your processes.
Once you have implemented your previously verified Werum PAS-X MES system, our team of experienced expert consultants will help with its validation. To ensure that this is done quickly and effectively we offer you our predefined, risk-based documentation package for the validation of computer systems.
Our on-site service supports your production operations wherever necessary. By working together with you closely, we can prevent longer downtimes. Our experts provide you with backup for days or weeks.
We save you time and effort during the transition to and commissioning of your PAS-X MES and during the hyper-care phase. We offer support for every project area: IT support, troubleshooting, and user training.
PAS-X content packages with preconfigured content ensure a fast start when implementing the PAS-X MES, thus enabling project running times and risks to be minimized.
Thanks to our PAS-X content packages you no longer have to start configuring PAS-X from scratch — you can get off to a good start with preconfigured templates. The templates are GMP-compliant, are based on the best practice of the pharmaceutical and biotechnology industry, and meet the needs of the PAS-X user community.
We support you in every phase of PAS-X MES implementation. We support you operationally and thus make time for you to concentrate on the essentials.
We support you in every phase of PAS-X implementation, from Ready to Fit and Build all the way to the Run phase. Within this framework, we take on many tasks that you had to carry out previously — and you save time and effort.
We offer you professional services to help with MBR (master batch record) development and are happy to advise you concerning the best way forward with drafting, creating, and checking high-quality MBRs.
MBR Studio — a complete solution for the cost-efficient creation of lean, high-quality, and process-optimized MBRs. The package consists of preconfigured PAS-X content packages, finished concepts for efficient MBR creation, and in-depth, first-hand PAS-X knowledge.
We offer consulting services for turnkey solutions — globally, for individual locations, and as part of the ongoing consultation.
Our comprehensive consulting services are perfectly matched to your specific requirements and support the entire lifecycle of your PAS-X MES project. We also offer services for strategic program management in the context of a global introduction.
Our PAS-X software product fulfills all the requirements of national and international licensing authorities
The PAS-X MES software and the associated development process fulfill all the requirements that the licensing authorities impose on the operation of computer systems in the regulated industry. For example, the functions of the PAS-X software fulfill the GMP requirements of the EU and the FDA.
Our international network of certified “PAS-X Endorsed Service Partners” offers pharmaceutical and biotech producers additional flexibility in the implementation of their MES projects.
Our certified service partners support you with their services during the implementation phase of your MES project. These services include master data parameterization, MBR development, validation, and support within the framework of on-site commissioning.