HomeNewsQuality / GMP

US FDA concludes inspection of Gland Pharma's Visakhapatnam facility with zero observations

US FDA concludes inspection of Gland Pharma's Visakhapatnam facility with zero observations

Drug maker Gland Pharma said that the United States Food and Drug Administration (US FDA) had inspected the company's API Facility at JNPC, Visakhapatnam, from January 23 to 27, 2023.

The drug maker further informed that the said inspection has been completed with 'zero' observations.

Hyderabad-based Gland Pharma has grown over the years from a contract manufacturer of small-volume liquid parenteral products, to become one of the largest and fastest-growing injectable-focused companies, with a global footprint across 60 countries, including the US, Europe, Canada, Australia, India, and other markets.

Read more on:
Gland Pharma US FDA
More news about: quality / gmp | Published by Sudeep Soparkar | January - 30 - 2023 | 917

Last news about this category


 

 

We use our own and third party cookies to produce statistical information and show you personalized advertising by analyzing your browsing, according to our COOKIES POLICY. If you continue visiting our Site, you accept its use.

More information: Privacy Policy

 pharmaindustrial-india.com - Professional magazine for pharma industry suppliers and lab technology - CEDRO members