Custom formulations and packaging solutions dedicated to OEM and contract services

We are proud to be able to offer our capabilities to fulfill Thermo Fisher Scientific's mission to enable our customers to make the world healthier, cleaner and safer. 

Whether you're looking for milligram, gram, or kilogram amounts, Thermo Fisher Scientific can support you with large-scale synthesis service and support at the level of purification, formulation, and format you need. 

  • High quality, reliable, responsive, and flexible
  • Dedicated to OEM and contract manufacturing
  • Experienced manufacturing facilities under ISO 9001 and ISO 13485
  • Well-established global manufacturing footprint and infrastructure
  • Known and trusted contract manufacturing partner

Industries served

  • Life science tools and reagents for basic and biomedical research
  • In vitro diagnostics (IVD) and molecular diagnostics (MDx)
  • Therapeutics

Special requests?Case study

OEM services and support

Leverage the expertise and infrastructure of Thermo Fisher Scientific, and have us manufacture products with your labels, in your packaging and inventoried in our facilities.

As a company providing thousands of products to customers globally, Thermo Fisher Scientific has developed expertise in supply chain management, product manufacturing and order fulfillment. And a as a vertically integrated organization, we have the ability to control reagent quality throughout the nucleic acid synthesis process.

Learn more about our OEM & Commercial Supply Services

GMP services

Powered by more than 100 years of combined experience, we offer dedicated ordering and fulfillment services that are integrated into your organization's systems and processes. Our capabilities extend to the production of oligonucleotide components for in vitro diagnostics (IVDs) and analyte-specific reagents (ASRs).

For more information, email


  • ISO 13485:2003
    The design, development (R&D), manufacture, distribution, of consumables and associated kits for life science research and for use as components of regulated kits manufactured and sold by diagnostic customers. (FM 561905)
  • ISO 9001:2008
    The design, development (R&D), manufacture, distribution, of consumables for life science research using our assay and oligo-related products. (FM 534534)

    The design, manufacture, distribution, installation, and support of instrument systems used for life science research. (FM 570472)
  • Certified GMP
    The FDA Good Manufacturing Practice Regulations require that manufacturers, processors, and packagers of drugs, medical devices, certain food items, and blood take proactive steps to ensure that their products are safe, pure, and effective.

Commercial manufacturing process*

Proposal ►

Development ►

Commercialization ►

  • Sign CDA
  • Assign PM
  • Gather reqs.
  • Assess gaps
  • Outline project
  • Supply agreement

Dev Support

  • Define strategies
  • Optimize product
  • Design packaging

Process Dev

  • Develop process
  • Validate process
  • Mfg pilot lots

Custom Mfg

  • Plan capacity
  • In-source material
  • Kitting, labeling
  • Optimize process


  • QC & compliance audits
  • Business reviews


  • Supply chain management
  • Relationshp management
* Process may be modified on a project-by-project basis.

For Research Use Only. Not for use in diagnostic procedures.