ACRO CMC QC Regulatory Support Center

Your all-in-one compliance engine to accelerate CMC quality control studies and regulatory submissions. We offer 3 specialized programs tailored to your needs!

Program 1: Eurofins-Validated Reports

Fast-track your drug development with validation reports from Eurofins, a trusted third-party institution. Gain thorough regulatory support with confidence and efficiency. (The Mycoplasma Rapid Detection Kit and CHO Host Cell DNA Quantitation Kit have successfully completed Eurofins validation. More validation reports are on the way — stay tuned.)

Program 2: ACRO QC Support Hub

From assay development to QC platform setup and optimization, our QC Support Hub offers end-to-end solutions addressing all key regulatory submission requirements.

Program 3: ACRO ThinkTank Sessions

Join in-depth sessions led by ACRO’s seasoned scientific team. Drawing on real-world project experience, these discussions provide actionable insights into complex biopharmaceutical quality control challenges.