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  Editorial
 WALK THE EXTRA MILE   
 Wednesday, April 2, 2025 
 Global recognition to the Indian Pharmacopoeia (IP) as a book of standard has been a major issue the Indian pharmaceutical exporters, including the merchant exporters, have been facing for a long time now. 
  Past Editorial...  
TODAY'S NEWS
18:00  [IST]Axsome Therapeutics to present positive phase 3 results of ACCORD-2 trial of AXS-05 in AD agitation and SYMPHONY trial of AXS-12 in narcolepsy at the 2025 AAN meeting
17:00  [IST]Signs identified that precede sudden arrhythmic death syndrome in young people
16:00  [IST]WHO brings countries together to test collective pandemic response
15:15  [IST]FTCCI, ASCI and SCC highlight on reducing cancer mortality with technology
15:00  [IST]UK MHRA approves eplontersen to treat adults with rare inherited nerve disease or polyneuropathy
14:50  [IST]Apollo Hospitals’ Health of the Nation 2025 report states new era of preventive care emerging
more news >>
Minebea_Sep24
TOP NEWS
08:00  [IST]Panel asks DoP to share data on quality checks and complaints against JAKs
08:00  [IST]Exporters raise alarm as new NOC norms trigger export disruption
08:00  [IST]TN DCA to get 18 new DIs next month to strengthen enforcement activities
08:00  [IST]Parliamentary Panel recommends setting up of institutional mechanism for integration of systems of medicine
08:00  [IST]Green hospitals evolving from being an option to a critical necessity to reduce environmental impact
08:00  [IST]Reciprocal tariff may pose significant challenge to growth of medical devices sector: AiMeD
more news >>
YESTERDAY'S NEWS
18:00  [IST]Intellia Therapeutics doses first patient in MAGNITUDE-2 phase 3 study of nexiguran ziclumeran
17:00  [IST]Pacira BioSciences begins patient dosing in phase 2 study evaluating safety and efficacy of PCRX-201 to treat osteoarthritis of the knee
16:00  [IST]Johnson & Johnson Global Survey reveals confidence in AI and medical technology to address personalized needs of aging population and alleviate burnout among HCPs
15:00  [IST]Vera Therapeutics completes full enrollment in pivotal ORIGIN phase 3 trial for Atacicept in patients with IgA nephropathy
14:00  [IST]Clinical Trials Information System designated as WHO primary registry
19:15  [IST]Supreme Court issues notice to Roche on risiplam matter
more news >>
INTERVIEW  
All DIs in TN are fully competent to inspect manufacturing units as per Revised Schedule M: MN Sridhar
MN Sridhar, director of the Tamil Nadu Drugs Control Department
Past Interviews...
 
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Will the introduction of Revised Schedule M by Union Health Ministry solve the issue of quality of Indian drugs?
 
 
 
   
 
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