Scientists have uncovered new details about iron from Antarctic icebergs. This iron, once thought to boost ocean life and absorb carbon, is...

The Indian government is amending drug regulations to expedite the approval process for clinical trials and bioavailability/bioequivalence ...

Hyderabad-based NiedlFree Technologies has developed a needle-free oral insulin spray called Ozulin, offering a painless alternative for di...

"With Shelcal's entry into OTC, the brand is poised to become the largest calcium supplement brand in India," Torrent Pharmaceuticals Direc...

The company has conducted bioavailability and bioequivalence (BA/BE) studies and is likely to submit the safety data to the drug regulator ...

In its meeting held this week, the SEC granted approval to the company to conduct bioavailability and bio equivalence (BA/BE) studies. “Cip...

Hetero Labs and Optimus Pharma had approached the drug regulatory authority last month seeking waivers from conducting local trials. Howeve...

Until now, it was widely thought that meteorites that bombarded early Earth were primarily responsible for the presence of "bioavailable" p...

The Switzerland-based firm, which is a clinical-stage oncology-focussed biopharmaceutical company, has received approval for its investigat...

Treating leukaemia cells with curcumin results in cancer cells dying more.

London, Feb 22 (IANS) People with major depressive disorder (MDD) have lower levels of naturally occurring arginine in their body than thei...

Cipla had based its application to the panel on the bioequivalence studies with Exubra, an inhalation drug and device combination that was ...

FDA inspections had found significant instances of misconduct and violations of federal regulations, including substitution and manipulatio...

The letter informs the sponsor that it must repeat the bioequivalence/bioavailability studies using an entity other than Semler at an accep...

This is another regulatory blow to the Indian drug industry, with several top pharmaceutical companies already under the watch of the US FD...

The drug regulator took the step after discovering that Sun didn’t have the requisite approval from the central government for operating th...

The company's Ahmedabad Clinical Pharmacology Unit successfully cleared US Food and Drug Administration audit with zero 483s/observations f...