Microbiology and in-vitro testing, under cGMP.

ACTA performs cGMP microbiological and in-vitro testing to meet your FDA compliance needs, for pharmaceutical products, water systems, and medical devices.

FDA Registered
DEA Licensed I to V
cGMP
Since 1990
ACTA microbiologist reviewing prepared media on a tablet in the microbiology media room
FIG. 01

Inside the lab

You reach the microbiologist leading the work, not a queue.

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.

In-house media room

Media prepared, staged, and tracked on site, not shipped in from somewhere else.

One quality system

Enumeration, specified organisms, and bioburden run under a single cGMP program.

Straight to the scientist

No intake layer between you and the microbiologist running your sample.

Bring us your micro project.

A specific test on a specific material. We will scope it, quote it, and a microbiologist will follow up. FDA-registered, DEA-licensed, cGMP since 1990.
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949-595-0641
info@actalabs.com