To more optimally address the growing demand for GMP peptides, AnaSpec has established a new facility dedicated to GMP manufacturing. Located adjacent to its current San Jose, California-based headquarters, the expansion provides an additional 5000 sq. ft. of dedicated GMP space.
	“The need for GMP-grade peptides is growing,” stated AnaSpec CEO, Dr. Frank Hong. “The expansion of our dedicated GMP manufacturing facilities will allow us to more fully address the stringent requirements of our customers.” AnaSpec has been synthesizing GMP-quality peptides for over 10 years. The new facility provides AnaSpec with an additional manufacturing site whose primary function is GMP production.
Fully equipped with large-scale synthesis and purification equipment as well as two class 10,000 clean rooms, AnaSpec’s state-of-the-art GMP facility is ideally suited to address our customers’ most demanding GMP peptide needs.

AnaSpec offers GMP peptides in milligram to kilogram quantities. Optimized for bulk API manufacturing, AnaSpec’s GMP peptide services offer >98% purity peptides with rigorous documentation and regulatory support including QC product release testing, stability studies, and full documentation for drug master files. AnaSpec holds a California Drug Manufacturing License (License #47174) and FDA Registration for GMP Drug Manufacturing (Registration #2951078). All GMP-grade peptide production strictly follows GMP and ISO-9002 guidelines.

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