Zydus receives EIR for the transdermal manufacturing facility
This facility underwent an inspection from 15th to 19th July 2024 and has been classified as Voluntary Action Indicated
This facility underwent an inspection from 15th to 19th July 2024 and has been classified as Voluntary Action Indicated
The USFDA inspection focused on evaluating the facility's adherence to global regulatory requirements and best practices
Jubilant HollisterStier is a subsidiary of Jubilant Pharma Holding
The company will take all necessary steps to work with USFDA towards earliest remediation of the above facility
The facility was inspected from May 7 to May 17, 2024
The USFDA has issued 15 observations pursuant to the completion of audit. JHSGP will submit an action plan on the observations
Operationally ready by 2029, it will be the Company’s first-ever facility to cover the full manufacturing process for ADCs
The USFDA has issued 5 observations pursuant to the completion of audit
The demand in Africa for COVID-19 vaccines has declined
Subscribe To Our Newsletter & Stay Updated