cGMP Distribution Services

Streamline your supply chain operations

Our Direct Materials Supply Chain Services have been developed based on decades of experience working with leading biopharmaceutical and life science companies that depend on us to meet applicable Current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP), and other global regulatory standards.

When partnering with customers, Thermo Scientific Production Chemicals and Services provides solutions to simplify and streamline overall production material supply chain and warehousing operations. Simplifying supply chain logistics for production chemicals and other direct materials enables companies to significantly increase risk mitigation, improve operational efficiencies, and reduce total cost of ownership.

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Explore our suite of supply chain services

Our supply chain services are scalable with an open architecture approach enabling customers to tailor a supply chain solution unique to their needs. We invite you to learn more about each individual service component – and how these services can help you focus on what matters most: bringing life-changing therapeutics to market.

Assurance of Supply Services
Discover how to assure supply availability with short lead times and high OTIF performance

Warehouse Efficiency Services
Understand how to improve speed and efficiency for inbound material receipt

Production Ready Services
See how to streamline direct material release processes and minimize on-site cGMP and GDP warehouse requirements

Importance of optimizing your supply chain

Managing the supply chain and mitigating risk for the direct materials used in bioproduction is complex. There are many details to be considered when partnering with a distributor, such as:

  • Protection of patient’s interests
  • Compliance with evolving regulations
  • Minimizing risks that impact the supply chain
  • Reducing total cost of ownership

Clean rooms meeting ISO 8 certification standards for material sampling (at select locations) cGMP/GDP facilities

Our audit-ready facilities are strategically placed in the United States and Europe, with global expansion plans. Facilities comply with the following requirements:

  • Meet ISO 9001: 2015 certification standards
  • Applicable cGMP guidelines
  • Clean rooms meet ISO 8 standards for material sampling (select locations)
  • Temperature mapped, controlled, and monitored
  • Cold storage at multiple temperature ranges
  • HAZMAT licenses for flammable, corrosive, poisonous, and oxidizer products
  • Humidity monitored
  • Built-in redundant processes

Related resources

Bioprocessing resources

Access a targeted collection of scientific application notes, case studies, posters, white papers and more for bioprocessing:

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