- LGM Pharma announces a 50% expansion and over $2 million investment in standalone Analytical Testing Services (ATS).
- The company introduces new suppository manufacturing capabilities to its portfolio.
LGM Pharma, a provider of tailored API and CDMO services for the full drug product lifecycle, has announced a significant enhancement of its capabilities. The company has made a 50% expansion and an investment exceeding $2 million in its standalone offering for Analytical Testing Services (ATS) alongside the introduction of new suppository manufacturing capabilities to its contract development and manufacturing (CDMO) portfolio.
In addition to analytical testing, the company provides comprehensive method development and validation services, as well as stability testing, including real-time and accelerated stability studies. LGM Pharma’s analytical laboratories, located at the CDMO’s facility in Irvine, California, are equipped with state-of-the-art chromatography and spectroscopy instrumentation, including ICP-MS and ICP-OES, to exceed the industry’s highest standards.
“Offering standalone analytical testing expands our agility and capacity to serve as a strategic resource for our pharmaceutical partners, providing them with flexibility to meet the precise needs of their expanding product portfolios,” said Prasad Raje, Ph.D., Chief Executive Officer at LGM Pharma. “With our continuum of robust and tailored support services, we enable pharmaceutical companies to get to market faster and achieve sustainable success in today’s complex market.”
Overview of outsourcing trends 
