ACTA is an FDA-registered, DEA-licensed, cGMP contract laboratory serving pharmaceutical and medical device manufacturers. The same credentialed scientists handle both, and they follow up on your project.
cGMP QC for APIs and drug products: assay and impurities by HPLC, elemental impurities, residual solvents, dissolution, endotoxin, water, stability, and method validation, to USP, BP, JP, EP, and ICH.
Pharmaceutical services →In-vitro biocompatibility (USP 87, ISO 10993-5 cytotoxicity) and bacterial endotoxin testing for medical devices, run under cGMP and 21 CFR Part 820 in an FDA-registered laboratory.
Medical device services →