Foothill Ranch, CA
For over thirty-five years, ACTA Laboratories has run comprehensive quality control for pharmaceutical and medical device companies, so you keep control over every stage of development, manufacturing, and testing.
ACTA is an FDA-registered, DEA-licensed, cGMP-compliant independent laboratory offering chemical, microbiological, and in-vitro testing, primarily to the pharmaceutical and medical device industries. We have passed numerous FDA inspections, including pre-approval inspections on NDA and ANDA products.
The industry is consolidating. Conglomerates buy up small labs and stop quoting small projects, and a new account can wait a month just to get into their system. ACTA stayed independent. We take the single test, scope it quickly, and follow up. Most of our largest accounts started as one small project.
You talk to the analyst running your method, not an account queue.
ACTA's chemistry analysts are extensively trained and routinely perform the USP General Chapters below. We also test to BP, EP, JP, FCC, AOAC, and ACS methods, or develop and validate a method for your product.
ACTA tests to USP, BP, JP, EP, FCC, AOAC, and ACS methods, to your validated method, or to a method we develop and validate for your material. Every project is run under cGMP and closes with a concise cGMP Certificate of Analysis.
