Our Facilities

Headquartered in Devens, Massachusetts, Johnson Matthey Pharmaceutical Services houses state-of-the-art, self-contained manufacturing suites...more

Technical Services

Johnson Matthey uses specialized technologies such as simulated moving bed chromatography (SMB), supercritical fluid chromatography (SFC), large-scale single-column chromatography, and catalytic technology screening to manufacture APIs...more

 

 

ABOUT US

Since its foundation as a precious metal assayer in 1817, Johnson Matthey has continued to develop new technology, demonstrating its ability to maintain world leadership by adapting constantly to the ever-changing needs of customers. Today the company employs around 7,800 people in over 30 countries across the globe, and its principal activities reflect its core skills. Johnson Matthey is a specialty chemicals company and a world leader in advanced materials technology. The group focuses on its core skills in catalysts, precious metals, fine chemicals and process technology, developing products and services that enhance the quality of life for millions around the world.

Johnson Matthey Pharma Services (JMPS) is your strategic partner in pharmaceutical product development and production. As your strategic partner, Johnson Matthey Pharma Services helps you develop and produce the world's highest quality active pharmaceutical ingredients, meet tight production deadlines, and speed new products to market. We provide API outsourcing solutions throughout the drug development process, from early stage discovery services to commercial manufacturing. We enable you to quickly succeed in your discovery, development and production of API every step of the way.

We assign a highly trained technical team to guide and assist you. Your Johnson Matthey Pharma Services scientific team is experienced in:

  • Sophisticated process development
  • State-of-the-art analytical methodologies
  • Process validation procedures
  • Responsive customer service
  • Manufacturing requirements for all Class I through V controlled substances
  • Registration in accordance with U.S. Drug Enforcement Administration guidelines
  • Requirements of the Food and Drug Administration's Good Manufacturing Practice (cGMP) Standards
  • Requirements of other international regulatory bodies

Whether it be designing, developing and optimizing synthetic routes, producing and/or scaling up intermediates and API, process development, process validation, or commercial manufacturing, we have the resources to get it done.