SOURCE: TriLink BioTechnologies
SAN DIEGO, CA--(Marketwired - Oct 22, 2013) - TriLink BioTechnologies TriLink (http://www.trilinkbiotech.com/) announced that it has signed an agreement with American Cleanroom Systems ACS (http://www.americancleanrooms.com/) and Kelchlin Construction to build a 2,000 square foot pharmaceutical cGMP (http://www.trilinkbiotech.com/GMP/) production suite within their San Diego facility.
The pharmaceutical cGMP production facility will contain nine labs and be equipped to manufacture and process mRNA, long RNA, aptamers, oligonucleotides, small molecules and nucleoside triphosphates. The project is scheduled to be complete in the first quarter of next year.
"Building a pharmaceutical cGMP production facility is the next logical step in expanding our quality system. Soon we will be able to support our customers at every stage from research to clinical trials and commercialization," said TriLink CEO, Richard Hogrefe, Ph.D. "ACS offered the quality and experience we were seeking and we're confident they are the right contractor to help us meet these goals."
TriLink manufactures custom oligonucleotides, modified nucleoside triphosphates and CleanAmp™ PCR products for the diagnostic and OEM markets. In addition, custom chemistry, long RNA and mRNA synthesis, contract research services and ISO/QSR compliant GMP production facilities are offered. TriLink's solutions help advance drug discovery and biomedical research. Founded in 1996, TriLink is a privately held firm based in San Diego, California and employs approximately 50 scientists and other professionals. For more information about the firm and products, visit our web site at www.trilinkbiotech.com.
ACS builds ISO4-8 class cleanrooms for the pharmaceutical and medical device industry. ACS cleanrooms offer innovative features like the ACS3000 monitoring system (patent pending), floor to ceiling glass walls, and the ACS wash-down wall system. ACS is located in Orange County CA. For more information visit www.americancleanrooms.com.