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Contract Manufacturing

Discover our contract manufacturing facilities and services

Potent therapies demand precision manufacturing 

Pharmaceutical and medical device companies that develop ready-to-infuse therapies — products that can often change a patient’s life — require specialized equipment and knowledge from a contract manufacturer.

From our facility in Larne, Northern Ireland, Terumo Blood and Cell Technologies offers contract manufacturing capabilities and solutions (also known as CMO or CDMO services) tailored to those complex needs. Our deep expertise in handling sensitive and potent formulations, with a focus on terminally sterile IV-bag solutions, is trusted by many of the top pharma and medtech companies in the world.

To discuss your IV solution contract manufacturing needs, contact us today.

Partner with confidence

Experience

40 years of experience in manufacturing ready-to-infuse solutions

Trust

Chosen by global pharmaceutical and medical device companies

Quality

cGMP ISO 13485-compliant facilities

Compliance

Licensed by MHRA and ANVISA and registered with FDA

Specialized CMO expertise infused in every bag

We offer white-label manufacturing for over 100 drug and medtech IV products for companies with global distributions.

Whether your product is in a research and development or a production phase, we can provide right-fit solutions with a dedication to the highest standard of quality.

Our teams are specialists in manufacturing:

  • IV therapies
  • Anticoagulants
  • Blood storage solutions
  • Perfusion solutions
  • Parenteral nutrition
  • Anesthetics and potent drugs

Our services

Dependable resources and customer solutions

  • Fill and finish for solutions in flexible IV containers (20 mL to 5,000 mL)
  • High-containment processing and dispensing for potent compounds (up to OEB5)
  • Terminal sterilization (autoclaves validated for IV containers)
  • Water for Injection (WFI) produced and tested on-site
  • Pre-sterilization foil overwrapping for light-sensitive formulations
  • Secondary packaging and labeling, including serialization
  • On-site testing lab with climate chambers
  • Stainless steel compounding tank systems
  • Semiautomated and fully automated filling lines
  • Automated sterilization and automated sealing
  • Gas purging systems for oxygen-sensitive products and other requirements during formulation
  • Overwrapping equipment for multiple packaging formats (polyethylene and foil overwrap)
  • Stability chambers with the capability to meet the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use guidelines for semipermeable containers
  • Product life cycle management
  • Product development support from container design to commercial validation
  • Process development and optimization, including support for commercial scale-up
  • Raw materials and finished goods testing
  • Technical and quality support, including stability and analytical testing for regulatory global submissions
  • Quality control testing and release support

If you’re looking for CMO IV solutions manufacturers, let’s discuss the many opportunities for partnership.

Email us at Larne.Sales@TerumoBCT.com or fill out the contact form.

Disclaimers and notes

Find information on ISO 13485.

CMO: contract manufacturing organization; CDMO: contract development and manufacturing organization; Medtech: medical technology; MHRA: Medicines and Healthcare products Regulatory Agency; FDA: U.S. Food and Drug Administration; ANVISA: Brazilian Health Regulatory Agency.

OEB: occupational exposure banding, a classification system for safe handling of hazardous chemicals.

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