Tag: Pharma Info
DoP the ceiling price fixation of 651 formulations generated annual savings of more than Rs. 3,500 crore in MAT
According to the drug price regulator, the moving annual turnover (MAT) for consumers on formulations for which the…
IPDMS 2.0 version is updated by NPPA with a number of modifications to assist industry with online filings.
The National Pharmaceutical Pricing Authority (NPPA) has made a number of changes to its Integrated Public Database Management…
To evaluate the PEF rate of lung function in asthma patients, Tenovi develops a cellular remote Peak Flow Metre that has been approved by the US FDA.
Tenovi offers Tenovi, a leader in US FDA-approved remote patient monitoring (RPM) solutions, recently announced the release of…
Sulbactam-durlobactam from Innoviva should be approved by the US FDA to treat ventilator-associated bacterial pneumonia and hospital-acquired bacterial pneumonia.
The US Food and Drug Administration’s (FDA) Antimicrobial Drugs Advisory Committee (AMDAC) unanimously voted 12-0 in favour of…
For Medicare users, Abbott’s FreeStyle Libre continuous glucose monitoring systems receive significantly greater coverage.
Abbott’s FreeStyle Libre portfolio, the most widely used and reasonably priced continuous glucose monitoring system (CGM) in the…
DCO India will begin a nationwide push to encourage the usage of generic medications.
The Drug Control Officers Welfare Association (DCO India) is preparing a pan-Indian campaign to amplify and promote the…
In persons with certain forms of adjuvant liver cancer, Roche reports that the Tecentriq + Avastin phase III IMbrave050 research lowers the likelihood of the cancer coming back.
Avastin (bevacizumab) plus Tecentriq (atezolizumab) showed a statistically significant improvement in recurrence-free survival (RFS) in patients with hepatocellular…
At MGM Healthcare in Chennai, a challenging small bowel transplant using an airlifted organ was completed.
An airlifted donor organ from Bengaluru was used in a difficult small bowel transplant by Dr. Anil Vaidya,…
CDSCO directs manufacturers & importers of Class C&D non-notified medical devices to submit application for license
The Central Drugs Standard Control Organisation (CDSCO) has instructed the manufacturers and importers of these devices to apply…
Due of the enormous increase in US FDA inspections, the pharmaceutical industry urgently has to establish a culture of quality, according to experts.
Experts have advised that it is urgently necessary to create a culture of quality in the pharmaceutical business…
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