Telangana: Gland Pharma has received Establishment Inspection Report (EIR) from the United States Food and Drug ...
Gland Pharma receives EIR from US FDA for Dundigal facility, indicating closure of inspection with no major concerns.
The Food and Drug Administration (FDA) has recently released two draft guidance documents (Artificial Intelligence-Enabled Device Software ...
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The Indian government wants micro, small, and medium drugmakers to meet WHO GMP standards by the end of 2025 or face shutdown ...
The generic drugs are procured from Indian drug makers that are certified by the WHO for following good manufacturing ...
The laxity in enforcing regulatory norms is one of the key issues that need to be addressed to check such incidents, especially with some of the drugs being made by small companies, experts said ...
On January 6, the U.S. Food and Drug Administration (FDA) issued long-awaited draft guidance regarding Establishing Sanitation Programs ...
It's one of many steps for the company as it builds the infrastructure for what "will change medicine everywhere in the world ...
Maintaining optimal health can often feel like an uphill battle in today’s fast-paced world, especially when managing blood ...
In today’s fast-paced world, maintaining good health has become increasingly challenging. With the rise in lifestyle-related ...
Adheres to requirements, including 21 CFR Part 820 and Good Manufacturing Practices.
Indian medical device manufacturers are enhancing GMP compliance and embracing proactive strategies to meet rising USFDA ...
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