Pharmaceutical & Biotech
GMP-compliant equipment for pharmaceutical manufacturing. Full validation support from development to production scale.
GMP compliant
Equipment designed and documented to meet FDA, EMA, and GMP requirements.
Validation support
Comprehensive IQ/OQ/PQ protocols and validation documentation packages.
Contained processing
Minimize operator exposure and cross-contamination with contained systems.
CIP/SIP ready
Clean-in-place and sterilize-in-place capable for efficient operation.
Built for pharmaceutical standards
Pharmaceutical manufacturing requires equipment that meets the highest standards for quality, documentation, and regulatory compliance. Our Swiss and German partners specialize in pharmaceutical-grade equipment with full validation support.
From MAVAG filter-dryers for API production to CEPA centrifuges for cell harvesting, we provide solutions that meet FDA, EMA, and international GMP requirements.
Pharmaceutical equipment
GMP-compliant solutions from trusted European manufacturers.
Specific use cases
How our equipment solves real pharmaceutical processing challenges.
API crystallization & isolation
Challenge
Active pharmaceutical ingredients must be isolated from reaction mixtures with high purity and consistent crystal form.
Solution
FUNDA® centrifugal disc filters provide high-throughput filtration with excellent cake washing for API isolation. For combined filtration and drying, MAVAG filter-dryers handle all steps in one contained vessel.
MAVAG FUNDA® filters / MAVAZWAG® filter-dryers
Cell harvesting
Challenge
Fermentation broths contain valuable products mixed with cell debris. Traditional filtration clogs quickly.
Solution
High-speed tubular centrifuges separate cells from broth continuously, without filter media. Ideal for E.coli, yeast, and mammalian cells.
CEPA high-speed centrifuges
Vaccine concentration
Challenge
Virus particles for vaccines are present in low concentrations and must be concentrated without damage.
Solution
Gentle centrifugal separation concentrates viruses while maintaining biological activity. No shear damage from pumps or filtration.
CEPA Z-series centrifuges
Blood fractionation
Challenge
Blood plasma contains multiple valuable proteins that must be separated and purified to pharmaceutical standards.
Solution
High-G centrifuges separate plasma fractions with precision. GMP-compliant designs meet blood product regulations.
CEPA GP centrifuges
Sterile filtration
Challenge
Final products must be sterile. Heat sterilization can damage sensitive biologics.
Solution
CIP/SIP capable centrifuges can be sterilized in place. Closed systems maintain sterility throughout processing.
CEPA GE centrifuges
Contained powder handling
Challenge
Potent APIs require containment to protect operators. Traditional open transfers create exposure risk.
Solution
Filter-dryers with glove ports, continuous liners, and split butterfly valves enable fully contained processing.
MAVAG contained systems
Why pharmaceutical companies choose us
Regulatory Expertise
- FDA DMF files available
- EU GMP compliance documentation
- Material certificates (3.1)
- Complete traceability
Validation Services
- Factory Acceptance Testing (FAT)
- Site Acceptance Testing (SAT)
- IQ/OQ/PQ protocols
- Process validation support
Trusted partners
We represent MAVAG of Switzerland for filtration and drying equipment, and CEPA of Germany for centrifuge technology. Both companies have decades of experience serving the pharmaceutical industry and maintain the highest quality standards.
As their partner in the Benelux region, we provide local support for equipment selection, installation, validation, and ongoing service.
We provide:
- Equipment selection and sizing
- GMP documentation packages
- FAT/SAT support
- Validation protocol development
- Spare parts and maintenance
Frequently asked questions
Our equipment comes with comprehensive documentation including material certificates (EN 10204 3.1), surface finish certificates, weld documentation, and FDA DMF references where available. We also provide IQ/OQ protocols and support your validation activities.
Pharmaceutical equipment inquiry?
Contact us for GMP-compliant solutions and validation support.
