Purolite Receives Accreditation of API Manufacturers From PDMA In Japan

Purolite has received an updated accreditation of active pharmaceutical ingredients (API) manufacturers certificate from the Pharmaceutical and Medical Devices Agency (PMDA) in Japan. The PMDA is equivalent to the Food and Drug Administration in the United States of America. “Accreditation of API manufactures” relates to good manufacturing practice (GMP) compliance.

Purolite has obtained this approval for its Victoria, Romania plant since 2006. The new certification extends to 2026.