USFDA closes inspection of Apitoria Pharma's facility, classifying it as 'Voluntary Action Indicated' after three observations.

Alkem Laboratories has received an EU GMP certificate from the Malta Medicines Authority for its Daman manufacturing facility. The certificate, valid for three years from December 9, 2025, confirms ...

Aurobindo Pharma Limited has announced that the United States Food and Drug Administration (USFDA) has classified Unit-V of its wholly owned subsidiary, Apitoria Pharma Private ...

The USFDA inspected the API manufacturing facility in Telangana between December 1 and December 12, 2025, following which a Form 483 with three observations was issued.

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China is rapidly reshaping the global manufacturing landscape through a powerful combination of industrial robotics, artificial intelligence, and large-scale factory ...

Gastrointestinal tolerability remained the dominant adverse-reaction cluster, aligning with established GLP‑1 receptor agonist class effects across dose ranges. A higher-dose signal of altered skin ...

Authorities seized large quantities of ingredients after flagging serious hygiene concerns at the facility.

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Manufacturer is integrating autonomy systems on its flagship R44 and R66 models.

National provider highlights critical gaps in AED programs across corporate, education, and public sectors. A green ...

Nearly four tonnes of unsafe dairy products were seized in Hyderabad, exposing a supply chain selling contaminated paneer to hotels and caterers.