Industri

Nimesulide and patient safety: Lessons from global drug...

Recently, the Indian Ministry of Health and Family Welfare issued a government ...

Granules Pharmaceuticals receives FDA tentative approva...

Granules Pharmaceuticals, a wholly owned subsidiary of Granules India, has rece...

Octapharma receives FDA approval for new Fibryga formul...

The approval offers healthcare providers with an additional option alongside the...

Day One concludes Mersana Therapeutics acquisition

The tender offer expired on 5 January 2026. The transaction involved purchasing ...

Sharp Sterile Manufacturing increases capacity with $28...

Sharp Sterile Manufacturing has announced a $28 million expansion of its site i...

Supriya Lifescience ramps up capacity and global readin...

Supriya Lifescience has built a strong global presence in Active Pharmaceutical...

We are cost-competitive and aligned with global ESG fra...

The biologics sector is very dependent on single-use products and containment s...

From MDD to MDR: How Usability Expectations Evolved — a...

1. Introduction: Usability Was Always There—MDR Just Started Asking th...

Cellenkos gains FDA orphan drug status for CK0804 to tr...

The condition has an estimated prevalence of 25,000 patients in the US and an an...

Zai Lab’s Augtyro receives NMPA approval for solid tumo...

The approval applies to patients whose disease is metastatic or locally advanced...

Sigachi Industries appoints Atul Dhavle as Chief People...

Sigachi Industries, a leading global manufacturer of pharmaceutical excipients ...

Separate license regime for bulk drugs, API and KSMs, u...

The government is considering a separate licensing framework for bulk drugs, ac...

Dr. Reddy’s launches Hevaxin, a novel recombinant Hepat...

Dr. Reddy’s Laboratories announced the launch of Hevaxin, a novel recombinant v...

Leadership imperative shaping India’s healthcare and ph...

India’s healthcare and pharmaceutical industries stand at an inflection point. ...

Arrowhead receives Health Canada authorisation for Rede...

The approval provides a new treatment option for this rare condition, which is l...

Takeda and Protagonist seek FDA approval for rusfertide...

The first-in-class, subcutaneously administered hepcidin mimetic peptide, rusfer...