
You can benefit from our many years of experience and our profound expertise. We’ve put together a selection of informative brochures, comprehensive white papers, and much more about the products, solutions, and services.
We guide you in your digital transformation in any phase: From the evaluation of your current digital maturity level with precise industry benchmarking to exploring quick wins with huge ROI potential. And of course, we support you with ongoing strategic consultancy to implement appropriate Pharma 4.0 components.
Get to know our services and your advantages for a Business Process Management Concept.
Transform your data into valuable knowledge by using Enterprise Manufacturing Intelligence
Learn how Lion.Execute can get you 30% higher machine availability.
Learn how to harmonize equipment interfaces and cetralize data using Lion.Manage.
Integrated serialization solutions Level 1 to level 5.
Get to know our track and trace solutions for Asia Pacific
Learn how mixed reality increases process efficiency by up to 30%.
Conquer the challenges of the shop floor processes and harmonize machine data on all IT levels.
Training, qualification, and validation services by experts.
Business process management at Top-10-global-pharma-companies
Learn how Novo Nordisk uses Lion to support an efficient biotech production
The Luye Pharma Case Study: How Luye Pharma solved serialization with Körber in no time.
The Occlutech Case Study: From requirement analysis to project implementation - we are your personal partner and your pharma technology expert
The Develco Case Study: Benefit from agile pharma project management combined with methodical execution according to GAMP®5
Machine Qualification Services for the Switch 75
Read in less than 10 minutes why CSA is not a replacement for CSV!
Particles, cosmetic defects, container integrity: whatever the task, we have the perfect inspection solution for your product.
High-performance inspection combined with de- and re-nesters: the perfect inspection system for large scale production lines.
Flexible inspection platform for small production batches - handles syringes and vials on the same machine
Comprehensive overview of the features and benefits of our semi-automatic inspection machine V90+
Eliminate false ejects with deep learning and make your efficient camera inspection even more powerful.
Remote Factory Acceptance Test: preparation, implementation, follow-up
Classroom training, web-based training, blended learning, virtual classroom - find the best suitable training concept for you.
The key to safe, fast, cost-effective validation of pharmaceutical inspection machines
Manual inspection: Our user friendly platform MVIC facilitates all manual inspection applications in the pharmaceutical market - in accordance with USP1790
Technical details of our flexible Switch 75 inspection machine (onepager)
Plug & inspect: Our mobile inspection unit for testing production parameters in laboratory environments, and suitable for countless other inspection and testing applications.
A simple and compact summary of the USP <1790> guideline, illustrating the individual test methods using Korber inspection machines as examples.
With Bubble-X, reliably distinguish glass particles and air bubbles in liquids - and thus avoid up to 50 % false rejects.
The latest updates on our pharma software products and services as well as our current customer success stories.
Out-of-the-box, instructor-led training modules that ensure the success of your pharma, biotech, and cell and gene therapy projects.
Learn how Electronic Batch Recording (EBR) enables the identification of the material at any point in time, thus facilitating ATMP compliance.
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Simplified documentation, accelerated workflows, and improved quality of products and processes with PAS-X MES
How to use artificial intelligence to uncover hidden business value in the regulated pharmaceutical and biotech industries.
Learn more about major saving areas with manufacturing execution systems (MES) and typical steps to evaluate ROI.
Reduce the number of manual operations and eliminate operator errors: Learn how a manufacturing execution system (MES) can address the unique production problems of cell & gene therapies.
How to save time and effort and avoid risk in your pharma or biotech production.
Learn how a manufacturing execution system (MES) addresss the unique biopharmaceutical supply chain challenges of cell & gene therapy logistics.
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Remote services and digital manufacturing keep your pharma & biotech operations running during crisis situations.
"By Christian Wölbeling and the ISPE Pharma 4.0™ Special Interest Group Working Group Leads The ISPE Pharma 4.0™ Special Interest Group (SIG) launched in 2015 to provide a road map for new challenges of digitalization, Industry 4.0, and the smart factory. The SIG addresses how pharmaceutical industry stakeholders, including regulatory authorities, can achieve benefits from Pharma 4.0™ initiatives. "
Get the full Gartner report
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Due to the large amount and complexity of the data to be considered and the diversity of the IT infrastructure with different source systems, the creation of the PQR is a time-consuming and challenging task. Get inspired how a validated software solution can support subject matter experts in the PQR process with automation, digitization, multivariate techniques and artificial intelligence.
Data management and analytics software substantially contributes to a successful process characterization.
PAS-X Weighing & Dispensing is a comprehensive package of software functionality, content and training services designed to improve the efficiency of your weighing operations.
PAS-X K.ME-IN offers you innovative biometric authentication solutions for pharma and biotech plants using fingerprint, iris scan, face recognition or a combination of those.
The Werum PAS-X MES manufacturing execution system helps you to digitize your pharma and biotech production.
PAS-X Data Access provides curated data from your PAS-X MES that can be consumed and visualized without detailed PAS-X knowledge.
PAS-X KPI is a lean, standalone software product for live monitoring of your production and packaging lines to improve the shop floor performance of pharma and biotech facilities.
PAS-X Plug & Produce allows you a fast and easy integration of machines and automation systems into a pharmaceutical or biotech production environment – a prerequisite for the implementation of many Industrie 4.0 solutions.
PAS-X Track & Trace provides line-controller-independent serialization and aggregation functionality for packaging processes to comply with anti-counterfeiting requirements for the pharmaceutical industry.
Werum PAS-X MES digitizes your cell & gene therapy manufacturing, targeting key challenges for cell & gene therapy companies.
Werum PAS-X Savvy revolutionizes managing, analyzing and reporting of your pharma and biotech process data.
Companies using Werum PAS-X MES have joined forces with Körber to help develop best-in-class MES technology, functionality and services.
Learn how we support you to optimize your packaging line and ensure right-first-time production.
Learn how Werum PAS-X Savvy helps you to evaluate Ambr® experiments as efficiently as possible, accelerating the whole biopharmaceutical process development.
Get familiar with our bioprocess software implementation strategies and accelerate your process data analytics.
Bioprocess data analytics to accelerate your product commercialization
The leading contract manufacturer SteriPack benefits from fast-track implementation and auto-batch release.
Interview with Sharp Packaging on the benefits digitization offers its customers by implementing PAS-X MES in their Heerenveen, Netherlands packaging plant.
Interview with AstraZeneca on the benefits of digitized processes for business resilience.
Deployment of Werum PAS-X KPI across packaging and bulk areas enables visibility of production processes and major OEE improvements.
Deployment of AstraZeneca's standard MES on the basis of PAS-X MES enables standardized business processes and enhanced data integrity.
The Japanese biotech company Unigen successfully took PAS-X MES into operation within a record time of only four months after completing the Fit phase.
A global pharmaceutical and biopharmaceutical leader relies on automated data collection and harmonization for multidimensional analysis of multiple batches across unit operations.
Consolidated data processing platform / Greatly reduced effort for data collection from different sources / Process intelligence supports efficient process development and faultless production runs
Dexa Medica, Indonesia’s leading pharma company, implemented Werum PAS-X MES out of the box in just ten months and largely remotely.
Powerful & Intuitive: High speed blistering for parenteral products and medical devices
More details on how Körber Xpert View supports you can be found in this brochure.
Ship up to 25% more products with precise product handling
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Effortless entry into the Monomaterial Toploading Packaging style
Effortless entry into the Monomaterial Toploading Packaging style
Small lots: How Sharp meets their challenge with Dividella NeoTOP
For the safe and loss-free transport of parenteral medication, nothing can shake the contents of our Safepack.
When it comes to sustainability, we are pioneers with our pharmaceutical packaging specialists.
Sustainable Pharma Packaging At four locations in Allschwil (Switzerland), Ejpovice (Czech Republic), Camden (New Jersey/USA) and San Juan (Puerto Rico), up to two billion folding cartons and package inserts for the pharmaceutical and biotech industries are produced annually by over 650 employees.
Packaging leaflets contain important information for patients.
Download the story about Körber's monomaterial solutions.
ISO 15378:2017: Primary packaging materials for medicinal products
Scope of certification: Rondo AG, 4123 Allschwil
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ISO 15378:2017: Primary packaging materials for medicinal products
Scope of certification: Rondo obaly s.r.o, 33701 Ejpovice
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ISO 9001:2015: Quality Management System
ISO 14001:2015: Environmental Management System
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Production Scheme: Physical separation (Transfer System)
PEFC ST 2002:2013
Chain of Custody of Forest Based Products-Requirements
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Forest Stewardship Council – Chain of Custody Standard reference: FSC-STD-40-004 (3.0), FSC-STD-40-003 (2.1)
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PEFC ST 2002:2013
Spotřebitelský řetězec lesních produktů – požadavky
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Forest Stewardship Council – Chain of Custody
Referenční normy: FSC-STD-40-004 (3.0), FSC-STD-40-003 (2.1)
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