Foothill Ranch, CA
ACTA is an FDA-registered, DEA-licensed, cGMP contract laboratory for pharmaceutical QA and QC. Identity, assay, and impurities by HPLC and GC-MS. Elemental impurities, residual solvents, dissolution, purified water, endotoxin, and microbial testing. From one specific test to a full stability program, you send us the material and a scientist scopes it.
Every method runs under cGMP against USP, BP, JP, and EP requirements, and you talk to the scientist who runs it. Pick a test for the detail, or send us the material and we scope it.
Not listed? ACTA runs many more compendial and custom methods across HPLC, GC, and ICP-MS. Tell us the test and the material and we will start a conversation. Request a Quote →
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 reach the scientists and regulatory staff who run the work, not a sales queue. Quotes typically go out in one working day.
One material, one test, no minimum program. The work larger labs decline is the work we build on.
FDA-registered and DEA-licensed for Schedules I to V, a scope few labs our size carry, with a clean cGMP inspection record.
A first test becomes method work, finished product testing, and stability. Your program expands with one lab that already knows your product.
