In the pharmaceutical industry, ensuring the safety, efficacy, and quality of drugs is an ongoing and intricate process. Independent testing laboratories, like Auriga Research, play a critical role ...
Only 4 out of 46 companies inspected showed 100% compliance with Revised Schedule M in Tamil Nadu: Peethaambaran Kunnathoor, Chennai Tuesday, November 19, 2024, 08:00 Hrs [IST] In ...
DGFT overhauls export policy through harmonisation with ITC (HS) 2022 to streamline pharma export process: Shardul Nautiyal, Mumbai Tuesday, November 19, 2024, 08:00 Hrs [IST] Wit ...
Unified mechanism under FSSAI for nutraceuticals would help rather than having two authorities: Expert: Gireesh Babu, New Delhi Tuesday, November 19, 2024, 08:00 Hrs [IST] A unifi ...
SEC recommends approval of additional indication for BMS' anti-cancer drug nivolumab: Gireesh Babu, New Delhi Tuesday, November 19, 2024, 08:00 Hrs [IST] The Subject Expert Commit ...
As part of a concerted effort to combat tuberculosis (TB) with a focus on climate change, Molbio Diagnostics, an innovator in global healthcare has contributed a donation of their state-of-the-art TB ...
Boston Pharmaceuticals, a clinical-stage biopharmaceutical company developing differentiated molecules addressing serious liver diseases, announced positive results from a phase 2 study evaluating the ...
Augurex Life Sciences, Quest Diagnostics collaborate to improve rheumatoid arthritis diagnosis and management: Vancouver, Canada Monday, November 18, 2024, 16:00 Hrs [IST] Augurex ...
Bristol Myers Squibb gets positive CHMP opinion for Opdivo plus Yervoy to treat adult with MSI-H or dMMR metastatic colorectal cancer: Princeton, New Jersey Monday, November 18, 2 ...
EMA encourages companies to submit type I variations for 2024 by end November 2024: Amsterdam, The Netherlands Monday, November 18, 2024, 14:00 Hrs [IST] European Medicines Agency ...
The Union Ministry of Ayush (MOA) will soon amend rules to regulate the retail sale outlets of the Ayurveda, Siddha and Unani (ASU) drugs in order to ensure safety, efficacy and quality of these ...
US FDA accepts for review the resubmission of sBLA for Dupixent to treat chronic spontaneous urticaria: Paris Monday, November 18, 2024, 11:00 Hrs [IST] The US Food and Drug Admin ...