Solutions

We have a solution for everything – and the corresponding experience. In our current seven areas of expertise, we are at your disposal with our comprehensive know-how.

All Solutions

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24/7 available for you: In our virtual showroom, we present our extensive portfolio and latest innovations. 

Software

Software

With our PAS-X Manufacturing Execution System (MES) and software solutions for Analysis, Track & Trace, Networked Factories, and Intelligent Packaging, we are the world's leading supplier and partner to the pharmaceutical and biotech industries.

Overview Software

Handling

Handling

We are specialists for complete handling systems for pharmaceutical and medical products. Our solutions are decisive in the field of contactless and safe transport of e.g. glass syringes.

Overview Handling

Inspection

Inspection

As the world's leading inspection expert, we develop solutions for the pharmaceutical and biotech industries. Our range of products extends from high-performance machines and semi-automatic machines to laboratory units and inspection applications for in-process control.

Overview Inspection

Deep learning with Seidenader Eject-X

Machine finder

Packaging materials

Packaging materials

As long-standing specialists, we develop packaging solutions for innovative and high-quality secondary pharmaceutical packaging made of cardboard. We offer you solutions for counterfeit protection, standard folding boxes and much more.

Overview Packaging materials

Services

You need help with a specific product or have questions about one of our areas of expertise? Take advantage of our extensive range of services, we will support you quickly and easily.

All Services

Packaging materials

Packaging materials

The demands on pharmaceutical packaging are high: it should be forgery-proof and childproof, but also compact and sustainable. Find out here how we make packaging future-proof.

Overview Packaging materials Services

About us

We at Körber in the Pharmaceuticals business area are the people to contact when it comes to pharmaceutical products. As a leading system provider, we advise our customers from the development and production to the inspection and packaging of their products.

All about us

MBR development: Tailored to your needs, from design to verification

An important aspect both during MES project implementation and later operation is the development of Master Batch Records (MBRs). We assist you in all phases, whether it’s the initial MBR creation process during project implementation or in the further MBR creation. 

You can use our MBR development portfolio as a comprehensive solution or select service packages that are tailored to your needs. In doing so, we always keep our common goal in mind: the creation of lean, high-quality, and process-optimized MBRs. 

Our portfolio consists of: 

  • Preconfigured PAS-X content packages with industry-specific best practice content 
  • Ready-made concepts and guidelines for efficient MBR creation and optimization
  • In-depth first-hand PAS-X knowledge 

Would you like to concentrate fully on your pharmaceutical production and leave the MBR design to the experts? Our Werum MBR Studio is an additional service to design your MBRs and will gladly take over the complete solution for you. The offering  has been created for customers who want to defer the complete MBR design process, from conceptualization to delivery, to the best-in-class service provider.  With established framework and processes, we ensure that your process is optimally mapped in the system.

Our services include:

  • The design, creation, and testing of MBR templates of certified quality
  • Creation of final MBRs on a large scale — also referred to as "MBR Factory"
  • Creation of global harmonization concepts and global MBR templates
  • MBR optimization

The three phases of MBR development

Our MBR development approach is based on  the design, creation, and verification of MBR templates.

The three phases in detail:

1. MBR design

We develop and document general design rules including data and design concept as well as acceptance criteria for later verification together with you on site.

2. MBR creation

MBR templates that cover the entire process in detail are created off-site  based on the defined data and design rules.

3. MBR verification

MBR templates are verified based on the criteria defined in the design phase.

After each phase, the resulting MBRs are compared with your business processes in an ongoing review procedure. This allows you to revise, redesign, and optimize the processes.

We check and verify the quality of your final MBRs by comparing them with the MBR design specification from the design phase, ensuring high-quality and efficient MBRs. 

Content packages and global templates 

Benefit from our templates and process libraries during MBR development to create MBR faster and accelerate projects to global MES deployment. 

The benefits of our content packages PAS-X Process Libraries and PAS-X Equipment Libraries:

  • Up to 80% faster in MBR creation 
  • Standardization of manufacturing processes
  • Cross-referencing / tracking capabilities
  • Migration capable
  • GMP-compliant by taking into account best practices from the pharmaceutical and biotech industries and implementing the requirements of the PAS-X user community 
  • Supports of cross-site process harmonization 
  • Lean MBR design

You can also benefit from our expertise in order to develop strategies and concepts for the global harmonization of your formulations or to support you in doing so. This allows you to establish best-practice standards of the highest quality on a global level that comply with global guidelines. You can also reduce your costs through centralized MBR templates and their maintenance. 

Your benefits

  • Lean, high-quality, and process-optimized MBRs
  • Time savings and lower costs
  • GMP-compliant and based on industry best practices 

Any questions?

Get in contact with us. We are happy to advise you about our solutions and services.

Get in contact

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