USFDA completes audit at Jubilant HollisterStier 2 Washington facilities
Written By : Ruchika Sharma
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2024-09-26 05:00 GMT | Update On 2024-09-26 05:00 GMT
Noida: Jubilant Pharmova Limited has announced that the United States Food and Drug Administration (USFDA) has concluded an audit of the Jubilant HollisterStier LLC’s Allergy immunotherapy facility and Contract manufacturing facility, both located in Spokane, Washington (USA) from September 18 to 25, 2024.
The inspection concluded with no observations. Jubilant HollisterStier LLC is a subsidiary of Jubilant Pharma Holding Inc., USA, which is a subsidiary of Jubilant Pharma Limited, Singapore, a wholly owned subsidiary of the company.
Jubilant HollisterStier LLC, based out of Spokane-Washington (USA) is a fully integrated contract manufacturing organization along with leading Allergy Immunotherapy provider in North America. The CMO business offers manufacturing services including sterile injectables (both liquid and lyophilization), ampoules and ophthalmics (Ointment, liquid and creams). With facilities in North America, Jubilant HollisterStier provides specialized manufacturing for the pharmaceutical and biopharmaceutical industries. The services include a full-range of support to streamline the manufacturing processes, from process qualifications through commercial release.
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