FDA launches PreCheck program to bring drug manufacturing back to US
The program seeks to boost regulatory predictability, support construction of US-based manufacturing sites
The program seeks to boost regulatory predictability, support construction of US-based manufacturing sites
A committee of two Joint Drugs Controllers has been constituted at CDSCO to monitor the process of inspection, reporting, and subsequent action to ensure compliance to the Drugs & Cosmetics Act, 1940
The partnership demonstrates increasing adoption of tetra data to create unrestricted innovation
The applicants will only have to get their Good Manufacturing Practices certification validated every five years to retain their licence
Lonza, a global manufacturing partner to the pharma, biotech and nutrition industries, has announced it will invest in additional drug product manufacturing capabilities in Switzerland
Transition to a fermentation-based globally integrated CDMO platform
The certification follows an inspection conducted by the Malta Medicines Authority between January 29, 2026, and February 3, 2026
We are building an AI-native operating system for pharma sales and distribution
Successful inspection outcome strengthens company’s regulatory compliance and manufacturing standards in China
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