Clinical Phase Solutions for CDMOs

Adaptable solutions for delivering clinical trial materials

Thermo Fisher Scientific supports CDMOs in clinical-phase drug development by providing GMP-compliant raw materials, analytical instruments, and regulatory knowledge to streamline clinical trial manufacturing and help accelerate time to market.

Regulatory Affairs Solutions

Regulatory solutions and an experienced team to help you navigate the evolving global regulatory environment.

Direct Materials Supply Chain Services

Solutions to simplify and streamline your overall production material supply chain and warehousing operations.

Portable Pharmaceutical QA/QC and Manufacturing Solutions

Helping to optimize quality coverage while minimizing time-consuming laboratory sampling tests. 

Clinical Phase resources

A comprehensive suite of services and solutions designed to enable your CDMO to navigate the complexities of clinical development and help deliver, GMP-compliant manufacturing, experienced process development, and reliable clinical trial material supply— helping your clients' drug development progress smoothly, efficiently, and in full regulatory compliance.

Featured resources

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