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Covid19 drug update | Mylan Secures Regulatory Approval for Remdesivir Lyophilized Powder for Injection 100 mg/vial in India for Restricted Emergency Use in COVID-19 Patients | Pharma News
HERTFORDSHIRE, England and PITTSBURGH and BANGALORE, India , July 6, 2020 / PRNewswire / -- Mylan N.V. (NASDAQ: MYL) today announced that the…
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Dr Reddy's partners with Fujifilm, GRA for favipiravir | Pharma News
Dr.Reddy's Laboratories on Wednesday announced partnership with Tokyo-based Fujifilm Corporation and Dubai-based Global Response Aid for th…
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News
Philips gets US FDA clearance for use of ultrasound portfolio to manage COVID-19-related lung & cardiac complications | Pharma News
Royal Philips, a global leader in health technology, announced the ultimate ultrasound solution for pediatric assessment, the latest addition for …
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Abbott gets US FDA emergency use authorization for COVID-19 molecular test on new Alinity m system | Pharma News
Abbott, a global healthcare leader, announced that the US Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for the …
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News
Dr Reddy's Labs Gets USFDA EIR For Srikakulam Formulations Plant | Pharma News
Hyderabad: Dr. Reddy's Laboratories Ltd on Wednesday said it has received an Establishment Inspection Report (EIR) from the US Food and Drug …
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Gilead ties up with Hetero drugs, 4 other generic drugmakers for Covid19 drug supply | Pharma News
Gilead Sciences Inc said on Tuesday it has signed non-exclusive licensing pacts with five generic drugmakers based in India and Pakistan to expan…
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Cipla Health partners Swiggy, Zomato, Dunzo to deliver wellness products | Pharma News
Startup Cipla Health, a subsidiary of Cipla, on Wednesday said it has partnered with Swiggy, Zomato and Dunzo for home deliveries of over-t…
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Strides
USFDA clears four Indian manufacturing plants in 10 days | Pharma News
MUMBAI: India’s leading drug companies have had their manufacturing facilities cleared in the last 10 days by the US Food and Drug Administration (…
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News
Dr Reddy's denies reports it is in talks with Gilead for Covid-19 antiviral | Pharma News
While media reports suggested that Hyderabad-based Dr Reddy's Laboratories is in the early stages of creating a generic version of anti-viral d…
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Indian Pharmaceutical Alliance commits to help fight Covid-19 | Pharma News
The national pharma lobby Indian Pharmaceutical Alliance (IPA) on Saturday said it will take every step to ensure that all coronavirus patients ge…
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FDA encourages recovered patients to donate plasma for development of blood-related therapies | Pharma News
As part of the all-of-America approach to fighting the COVID-19 pandemic, the U.S. Food and Drug Administration has been working with partners acr…
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Dr Reddy’s Laboratories share price slips 2% on USFDA observations
United States Food and Drug Administration (USFDA) issued a Form 483 with five observations to the company's API manufacturing plant at Srikaku…
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Dr. Reddy’s receives a warning letter | Pharma News | Pharma Udyog
Dr. Reddy’s Laboratories is one the renowned pharmaceutical company in the Telugu states. Seems like there is a slight tension in the company…
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Jubilant Life Sciences in plans to split pharma and life science ingredient businesses | Pharma News | Pharma Udyog
Noida-based Jubilant Life Sciences Ltd plans to demerge its pharmaceuticals and life science ingredient businesses as part of its second phase of r…
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Pfizer
Pfizer in talks to merge off its patent drugs business with Mylan | Pharma News | Pharma Udyog
Bengaluru: Pfizer Inc is in talks to merge its off-patent drugs business with Mylan NV in a stock deal, the Wall Street Journal reported on Sat…
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FDA approves new treatments for heart disease caused by a serious rare disease, transthyretin mediated amyloidosis | Pharma News | FDA
On May 3, the U.S. Food and Drug Administration approved Vyndaqel (tafamidis meglumine) and Vyndamax (tafamidis) capsules for the treatment of the h…
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News
USFDA retains OAI status for Indoco's Goa plant | Pharma News | FDA
As per the USFDA, observations have been made after inspection of a facility in response to Form 483. An FDA Form 483 notifies the company's man…
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News
Dr Reddy's launches erectile dysfunction treatment drug in US
Dr Reddy's Laboratories on Wednesday announced launch of Tadalafil tablets, used to treat erectile dysfunction, in the US market. The appro…
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Sun Pharma
Sun Pharma gets one 483 for Baska facility, Company says responded to FDA
MUMBAI: India's largest drug maker Sun Pharma on Monday said that it has received letter 483 (an observation of deviation in manufacturing pr…
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Sun Pharma
Sun Pharma auditor files case against Macquarie with Economic Offences Wing
The Mumbai Police's Economic Offences Wing (EOW) has initiated an inquiry against Macquarie broking house on the basis of complaint registere…
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