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After US, India to probe Ranbaxy's documents

After US, India to probe Ranbaxy’s documents SUSHMI DEY New Delhi, 22 May Health ministry tells DCGI to examine past dossiers, drug applications In what could be the beginning of fresh......

Drug makers seek out-of-court settlement in clinical trial cases

In order to keep pace with the government’s healthcare agenda, the pharmaceutical sector wants research work to go on, at any cost. In a letter to health minister Harsh Vardhan, the Indian......

Why is Novartis likely to lose Tiamulin drug licence?

Swiss drug maker Novartis is likely to face legal action for allegedly faking documents to seek registration of its veterinary product Tiamulin Hydrogen Fumarate (80 per cent granules) in India.......

Ranbaxy whistle-blower to talk on quality of Made-in-India drugs

The concerns surrounding drug manufacturing practices in India appear to have reached foreign shores, beyond the international regulators’ domain.  Ranbaxy whistle-blower Dinesh Thakur,......

Keep us in loop before any FDA swoop, India tells US

Inspections only in domestic authorities’ presence, visiting US drug regulator told Taking a tough stand on the ongoing regulatory issues faced by the domestic pharmaceutical industry because......

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