Pharmacy India
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The US Food and Drug Administration’s (FDA) Antimicrobial Drugs Advisory Committee (AMDAC) unanimously voted 12-0 in favour of approval of sulbactam-durlobactam for the treatment of adults with ventilator-associated bacterial pneumonia and hospital-acquired bacterial pneumonia caused by susceptible strains, according to…
Abbott’s FreeStyle Libre portfolio, the most widely used and reasonably priced continuous glucose monitoring system (CGM) in the United States, will now make more Medicare beneficiaries than ever before eligible for reimbursement when using it. According to Jared Watkin, executive…
Examination Date & Schedule for Graduate Pharmacy Aptitude Test (GPAT- 2023)The Graduate Pharmacy Aptitude Test (GPAT) is a National Level Entrance Examination for entry into M.Pharma programmes.It is hereby informed that National Testing Agency (NTA) will now be conducting GPAT-2023…
The Drug Control Officers Welfare Association (DCO India) is preparing a pan-Indian campaign to amplify and promote the use of generic formulations in support of the Union government’s programmes for generic medicine promotion. The drug control officers, who are concentrating…
Avastin (bevacizumab) plus Tecentriq (atezolizumab) showed a statistically significant improvement in recurrence-free survival (RFS) in patients with hepatocellular carcinoma (HCC) at high risk of disease recurrence following liver resection or ablation with the intention of curing the disease, according to…
An airlifted donor organ from Bengaluru was used in a difficult small bowel transplant by Dr. Anil Vaidya, director and senior consultant of multi-visceral transplant surgeon at MGM Healthcare in Chennai. Under the direction of Dr Anil Vaidya, who is…
The Central Drugs Standard Control Organisation (CDSCO) has instructed the manufacturers and importers of these devices to apply for grant of manufacturing or import licence with all necessary documents and fees in accordance with the regulation in an effort to…
Experts have advised that it is urgently necessary to create a culture of quality in the pharmaceutical business in view of the sharp increase in US FDA inspections for compliance and quality assurance. They did this by highlighting the fall…
The US Food and Drug Administration (FDA) has responded completely to Alvotech’s Biologics Licence Application (BLA) for AVT02, a high-concentration biosimilar candidate for Humira (adalimumab), according to a press release from the international biotech company Alvotech. The FDA’s reinspection of…
To combat fake pharmaceuticals, it is absolutely necessary for patients to be aware of websites that provide medications at discounts. The public’s health is at risk because to the parallel trade of real medical supplies that are moved without the…
