Last Updated on October 6, 2024 by The Health Master
USFDA Inspection
Hyderabad, India – Laurus Labs Ltd., a prominent pharmaceutical and biotech company, has announced a significant achievement. The company’s API manufacturing facility in Hyderabad has successfully passed a rigorous US Food and Drug Administration inspection (USFDA inspection).
Zero Observations, a Clear Indicator of Excellence
The USFDA inspection, which took place from September 9th to 13th, was designed to assess the facility’s compliance with stringent global regulatory standards and best practices.
The outcome was impressive: no Form 483 observations were issued.
This is a clear indication of the facility’s adherence to the highest quality standards.
A Crucial Facility for Global Healthcare
Laurus Labs‘ API manufacturing facility, located at DS-1, IKP Knowledge Park in Genome Valley, Shameerpet, Telangana, plays a pivotal role in the development of Active Pharmaceutical Ingredients (APIs).
These are the essential components of many medications used worldwide.
Laurus Labs
Laurus Labs, headquartered in Hyderabad, India, is a leading pharmaceutical company with a strong focus on research and development.
The company specializes in critical therapeutic areas such as anti-retroviral, Hepatitis C, and Oncology drugs.
Global Recognition
The successful completion of the USFDA inspection further solidifies Laurus Labs’ reputation as a trusted and reliable supplier of pharmaceutical products.
The company’s manufacturing facilities are approved by major regulatory authorities worldwide, including the USFDA, WHO-Geneva, and UK-MHRA.
Disclaimer: This article contains information derived from the source mentioned below. Our team utilized an AI language model to rewrite and present the news or article in a unique format.
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