Nandita Vijayasimha, Bengaluru Monday, January 12, 2026, 08:00 Hrs [IST] ...
MSMEs need handholding to implement online submission of CDSCO mandated WHO-GMP CoPP: BDMAI: Shardul Nautiyal, Mumbai Monday, January 12, 2026, 08:00 Hrs [IST] Pharma MSMEs need a ...
Telangana DCA’s 2025 annual action taken report highlights expansion of enforcement & global regulatory synergy: Peethaambaran Kunnathoor, Chennai Monday, January 12, 2026, 08:0 ...
Imports of bulk drugs and intermediates to India registered a decline of 2.81% in the month of November, 2025, while exports grew 11% during the month as compared to the same period of previous year.
DoP calls for proposals to set up common facilities for medical device clusters: Gireesh Babu, New Delhi Monday, January 12, 2026, 08:00 Hrs [IST] The Department of Pharmaceutical ...
BDCDA seeks reconsideration of Karnataka Drugs & Cosmetics Rules Amendments: Nandita Vijayasimha, Bengaluru Saturday, January ...
Stevenage, United Kingdom Saturday, January 10, 2026, 14:00 Hrs [IST] ...
MRM Health receives US FDA IND clearance to initiate phase 2b trial of MH002 in mild-to-moderate ulcerative colitis: Ghent, Belgium Saturday, January 10, 2026, 16:00 Hrs [IST] MRM ...
Moving Biotech receives US FDA’s IND clearance for 4P004; strengthens its position as a leading innovator in disease-modifying osteoarthritis therapeutics: Lille, France Saturd ...
Opinion
Vanda Pharma announces receipt of US FDA decision letter on Hetlioz sNDA for jet lag disorder
Vanda Pharma announces receipt of US FDA decision letter on Hetlioz sNDA for jet lag disorder: Washington Saturday, January 10, 2026, 13:00 Hrs [IST] Vanda Pharmaceuticals Inc. (V ...
PharmaForceIQ acquires Aktana to deliver unparalleled cross-functional engagement impact for pharma sector: Miami Saturday, January 10, 2026, 15:00 Hrs [IST] PharmaForceIQ, an end ...
US FDA grants fast track designation to Complement Therapeutics’ gene therapy candidate CTx001 to treat geographic atrophy: Munich Saturday, January 10, 2026, 17:00 Hrs [IST] Co ...
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