A central hub for GMP excellence

Our state-of-the-art Pharma GMP Hub brings together value-added services, GMP manufacturing and product expertise, all at a single, dedicated site.

Your trusted partner for GMP-compliant solutions

The demand for high-quality GMP services in the biopharmaceuticaland pharmaceuticalindustry is growing rapidly.Our new Pharma GMP Hub is our response: A purpose-built, state-of-the-art facility designed to meet the complex needs of our customers and suppliers by providing pharma value-added-services and biopharma value-added-services.
Why choose our Pharma GMP Hub?
Our GMP Hub integrates product development, production, packaging, and testing – all under one roof. We deliver flexible, scalable, and fully compliant solutions that help accelerate your development timelines without compromising on quality or regulatory integrity. These GMP services encompass pharma GMP services, biopharma GMP services, and GMP value-added services.
We combine our deep technical expertise with end-to-end service capabilities to bring your innovations to market – faster and safer. As a leader in pharma services and biopharma services, we deliver pharma customized solutions tailored to your needs.
Contact our pharma experts
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Our state-of-the-art facility

Our facility meets the highest international standards for cGMP and GMP pharmaceuticals. We offer:
  • GMP-compliant operations
  • EXCiPACT in reapplication
  • ISO 9001:2015
  • Cleanrooms: ISO Class 7 (GMP Class C) and ISO Class 8 (GMP Class D)
  • FSSC 22000 certification
  • GDP-certified warehouse with 1,500 pallet spaces
Sustainability built in
Equipped with a 77.5 kWp solar power plant, our site actively contributes to more sustainable pharmaceutical manufacturing processes.

Our products and services

We offer a comprehensive portfolio of GMP-compliant products and services tailored to the specific needs of the pharmaceutical and biopharmaceutical industries – including both pharma services and biopharma services.
Custom formulation and manufacturing of biological buffers tailored to precise process requirements. Our biopharma buffers are developed as part of our specialized biopharma buffer services and biobuffers services
  • GMP-grade buffers​
  • Certified facility (ISO 9001:2015 and EXCiPACT in reapplication)​
  • Class C clean room for manufacturing and filling​
  • Batch sizes: 1,000L to 10,000L (smaller on request)​
  • Packaging options: 150mL to 1,000L​
  • ATEX rooms ​
  • Full biopharma regulatory documentation with custom Certificates of Analysis (CoAs) and additional customer specific testing if required
Offering
  • Custom buffers for biopharma applications​
  • WFI-based manufacturing for high-purity solutions​
  • Full range: formulation, upstream, downstream, and CIP/SIP buffers​
  • Packaging: 2D/3D bio-bags, jerricans, IBCs​
  • Monograph-compliant testing, with optional low endotoxin validation​
  • Tailored sampling plans per customer needs​
  • Supply chain management with secure transport including returnable rigid outer containers​
  • Secure transport in rigid containers​
  • GDP-compliant logistics with temperature/humidity control​
  • Detailed CoA and documentation provided with every order
Buffer types
At Brenntag, we understand that your buffer needs are unique and often require customization.​ Here you find a selection of buffer types and related solutions we commonly provide.
Buffer Solutions
  • Tris buffers​
  • HEPES buffers​
  • MES buffers​
  • Phosphate buffers​
  • Citrate buffers ​
  • Acetate buffers
Other Chemical Solutions
  • Iso-Propyl alcohol solutions​
  • Sodium hydroxide Solutions​
  • Ethanol solutions​
  • Ammonium sulfate and ammonium chloride solutions​
  • WFI for further processing
We provide high-precision repackaging solutions to maintain product integrity throughout the supply chain. Our GMP powder down-packing capabilities include both powder repacking GMP and powder downpacking GMP services.
  • GMP repacking of excipients and critical raw materials
  • Down-packing from bulk to standard or custom formats​
  • Packaging formats available from 1kg to 30kg
  • Flexible repacking into HDPE drums, cartons, bags​
  • Non-GMP options for non-critical materials​
  • Support for cleanroom-compliant packaging​
  • QP-supervised testing and product release​
  • Batch documentation provided with every order
We offer accurate and controlled blending of liquids, tailored to client-specific formulations. Our services encompass liquid mixing pharma and liquid blending pharma to support a broad range of applications and production needs.
  • Custom liquid blends for excipients, intermediates, and starting materials​
  • GMP and non-GMP blending available​
  • Packaging options: tankers, IBCs, drums, buckets, cans, 2D/3D bio-bags, bottles​
  • Full documentation included with each batch​
  • Monograph testing (Ph. Eur., USP, JP, etc.)​
  • Specialized testing: endotoxins, bioburden, elemental impurities, micro, stability, method development
Ultra-pure water for biopharma processing
  • Available in flexible formats (bulks, sterile single use bags, and other custom containers)​
  • GDP-compliant transport and climate-controlled storage​
  • Meets GMP, EP, and USP standards for biopharma use​
  • Validated systems ensure traceability and audit readiness​
  • Customer-specific sampling available
GMP-grade caustic solution for cleaning, and in-process use
  • Tested to meet multi-compendial including USP, EP, GP quality​​
  • Low endotoxin/bioburden < 2.0 EU/ml​
  • Sterile filtered using 0.2 µm filter (biopharma grade)​
  • Manufactured with multi-compendial WFI
  • Manufactured using multi-compendial sodium hydroxide pellets
  • Available in various concentrations ranging from 50% to 0,1%
  • Flexible packaging options: tankers, drums, IBCs, isotainers, 2D/3D biobags, bottles, customer tailor-made
  • Customer-specific sampling available​
We provide comprehensive in-house testing to ensure batch consistency, product quality, and full regulatory compliance. Our analytical services include pharma analytical testing according to EP and USP standards, ensuring complete monograph compliance
  • Custom testing for batch release and material compliance​
  • Pharmacopoeia testing (USP, EP, JP, BP, CP, others)​
  • Endotoxin, bioburden, and microbiological testing for raw materials and excipients​
  • Additional services: elemental impurities, stability, method development, validation​
  • Full documentation included with all products
GMP-compliant sampling and storage services to ensure material integrity, traceability and regulatory compliance
  • Sampling of all pharma critical raw materials and excipients
  • Sampling conducting under strict quality and regulatory controls in a Class C clean room
  • Automated storage of samples utilizing specialized Kardex system
  • Distribution of samples globally
  • Sample pack sizes ranging from 5g to 1kg
  • Small scale commercial sampling available 1kg to 25kg
R&D for method development and batch testing
  • R&D development of buffers and buffer concentrates
  • Stability testing and custom test parameters​
  • Formulation support for pharmaceutical applications​
  • NPD labs for testing new formulations​
  • Raw material purification and development
Business man Gearoid O'Rourke portrait image
“A GMP-compliant reliable partner for biopharma companies seeking rapid scale-up, regulatory readiness and consistent quality.”

Gearoid O'Rourke

Director Value Added Services Pharma EMEA

How we enhance your business

GMP compliance
Fully GMP certified, ensuring regulatory confidence and consistent product quality.
Biopharma-focused
Purpose-built to meet the unique needs of biotech and pharma clients, including complex products.
Integrated services
Streamlined services under one roof, from formulation to production and packaging.
Scalable and flexible
Supports both small-batch and commercial-scale operations. Adaptable to early-phase and mature pipelines.
Strategic location
Based in Czechia, offering optimized logistics and market access within the EU and EMEA regions.
Technical expertise
Supported by Brenntag’s scientific, regulatory and supply chain know-how.
Speed to market
Efficient onboarding and rapid execution, helping you accelerate your development timelines.
Partnership-oriented
A collaborative, solution-focused approach to long-term customer success.
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Let’s move forward, together

Whether you’re launching a new therapy or scaling up an existing pipeline, our Pharma GMP Hub is ready to support your next step - with precision, flexibility and confidence.
Contact our Pharma team today to learn more or to schedule a consultation.