Vishal highlighted the struggles of small-budget films and emphasized women's self-defense. While not ready for politics, he called for tax relief for Tamil cinema in the Union Budget.

The U.S. Food and Drug Administration has approved Journavx (suzetrigine) 50 milligram oral tablets, marking the introduction of a first-in-class non-opioid analgesic designed to treat moderate to ...

The certified period of Japanese Food Supporter is set for two years from the day of certification. (Need to apply for renewing the certification to continue after 2 years.) Requirements for ...

Sotax India delivered talk on various aspects of Dissolution Science and Drug Development. The event also had a live demonstration of Sotax USP4 Dissolution Apparatus. Thiru. M N Sridhar, Director of ...

mandated the use of the ISI mark on insulated food containers, thermo flasks, and bottles, but the BIS is yet to gain registration for product certification in Tamil Nadu. With manufacturers in ...

The Company has also submitted a New Drug Application (NDA ... would be the first oral on-demand treatment for HAE in Japan. "The submission of our NDA for sebetralstat in Japan represents ...

Orphan drug designation paves the way for potential of sebetralstat to be first oral on-demand treatment for HAE in Japan– – Submission advances Company ... require either intravenous or subcutaneous ...

The Food and Drug Administration (FDA or we) is amending the color additive regulations to provide for the safe use of myoglobin as a color additive in ground meat and ground poultry analogue products ...

Raritan: Johnson & Johnson has announced it has initiated the submission of an original New Drug Application with the U.S. Food and Drug Administration (FDA) for TAR-200 for the treatment of patients ...

Companies say they are working to update their products to comply with the Food and Drug Administration's decision Wednesday to ban the artificial food dye Red 3, after the agency said it was ...