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The Pharmacopoeia Commission of Indian Medicine and Homoeopathy (PCIM&H) may soon start developing pharmacopoeia standards for the Ayurvedic, Siddha, Unani, and Homoeopathic medications under the “One Herb One Standard” (OHOS) among other projects during the budget year 2023–2024. According to…
The US Food and Drug Administration has approved the company’s investigational new drug (IND) application for CABA-201, a fully human CD19-CAR T cell investigational therapy that contains the 4-1BB protein, according to Cabaletta Bio, Inc., a clinical-stage biotechnology company focused…
Applications are invited from suitable candidates for a Junior Research Fellow (JRF) position to work on the following project sponsored by ICMR, under the supervision of Venkata Vamsi Krishna Venuganti, Department of Pharmacy, BITS Pilani, Hyderabad campus and Dr Vishal…
The phase 2 recruitment for Hansa Biopharma’s imlifidase research in Guillain-Barré syndrome has been completed, according to the company, a pioneer in enzyme technology for uncommon immunological disorders (GBS). The second half of 2023 is anticipated to see the release…
The Pharmacy Council of India (PCI), a statutory body established for the regulation of pharmacy education, profession, and practise in the nation, has been reorganised. An expert committee has been established by the Union Ministry of Health to evaluate the…
In a patent dispute involving the former’s diabetes drug linagliptin, a single judge of the Delhi High Court declined to grant an interim injunction in favour of German pharmaceutical giant Boehringer Ingelheim against Indian generic manufacturers, noting that the patent…
According to the National AIDS Control Organization, the risk of HIV transmission through blood transfusions has decreased from 15% to less than 1%. (NACO). It has been estimated that heterosexual routes account for over 83% of all transmission in India….
The US Food and Drug Administration (FDA) has fully approved Keytruda, Merck’s anti-PD-1 therapy, for the treatment of adult and paediatric patients with unresectable or metastatic microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) solid tumours, as determined by an…
In order to treat persons with aortic regurgitation or stenosis, Abbott announced that the US Food and Drug Administration (FDA) has approved the company’s Epic Max stented tissue valve. With an enhanced design to further increase valve blood flow, this…
The first naloxone medication to be approved for use without a prescription is Narcan, a 4 milligramme (mg) naloxone hydrochloride nasal spray, according to the US Food and Drug Administration (FDA). The conventional treatment for opioid overdose is naloxone, a…
