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Netherlands startup and Oxford Nanopore Technologies The world’s first nanopore sequencing-based technology for ultra-sensitive detection of circulating tumour DNA has been made available to developers by Cyclomics (ctDNA). The procedure finds and evaluates cell-free DNA (cfDNA) in the blood. As…
The first participant in Alterity Therapeutics’ phase 2 clinical trial of ATH434 in multiple system atrophy (MSA), a rare and severely handicapping Parkinson’s disease, has been dosed in the US, according to the biotechnology company’s announcement. Alterity Therapeutics is dedicated…
What is H3N2 Influenza? A subtype of influenza called H3N2 In India, a virus has been rapidly spreading, resulting in 90 cases and 2 fatalities thus far. According to reports, the ailment causes a fever that lasts three to five days…
As part of the Pharmacovigilance Plan of India, the National Medical Commission (NMC) has ordered all accredited medical colleges and independent PG institutions to enrol as Adverse Drug Reaction Monitoring Centers (AMCs) with the Indian Pharmacopoeia Commission (IPC) as soon…
A vulnerable population in India is now being helped to survive abrupt cardiac arrests thanks to MedLern HeartCode full training. The MedLern platform is made exclusively for hospitals in India to standardise and enhance training for their medical staff. It…
The first patient with hepatocellular carcinoma (HCC) has begun treatment in phase 2a with the candidate drug fostroxacitabine bralpamide (fostrox) in combination with Lenvima, according to Medivir AB, a pharmaceutical company dedicated to creating novel cancer treatments in regions with…
BRIDGEWATER, N.J.–(BUSINESS WIRE)– Amneal Pharmaceuticals, Inc. (NYSE: AMRX) today announced the U.S. Food and Drug Administration (FDA) has accepted for review the Abbreviated New Drug Application (ANDA) for naloxone hydrochloride nasal spray, USP, 4mg, which is the generic version of Narcan® and…
One of the top manufacturers of minimally invasive structural heart disease devices, Occlutech Holding AG (Occlutech), has announced the enrollment of the first patient in the FROST-HF study. In the FROST-HF study, patients with heart failure with either preserved ejection…
Zydus Lifesciences Limited (including its subsidiaries/affiliates, hereafter referred to as “Zydus”) has received final approval from the United States Food and Drug Administration (USFDA) for Lenalidomide Capsules, 2.5 mg and 20 mg (USRLD: Revlimid® Capsules). Lenalidomide Capsules are used to…
The Pharmaceuticals Export Promotion Council of India (Pharmexcil) has urged its member companies to submit their expressions of interest (EOI) to export levothyroxine and levonorgestrel from India if they have operations in Latin American Countries (LAC) or are interested in…
