ACTA performs cGMP microbiological and in-vitro testing to meet your FDA compliance needs, for pharmaceutical products, water systems, and medical devices.
ACTA offers comprehensive microbiological services, including in-vitro biological reactivity and cytotoxicity for medical devices, all under cGMP with a concise Certificate of Analysis.
Inside the lab
ACTA runs its own microbiology suite. Media is prepared, staged, and tracked in house, so enumeration, specified organisms, and bioburden all sit on one cGMP quality system.
Media prepared, staged, and tracked on site, not shipped in from somewhere else.
Enumeration, specified organisms, and bioburden run under a single cGMP program.
No intake layer between you and the microbiologist running your sample.
