Marksans Pharma gets EIR from USFDA for its Goa facility Ruby Khatun Khatun10 Oct 2017 11:17 AM ISTNew Delhi: Drug firm Marksans Pharma said it has received Establishment Inspection Report (EIR) from the US health regulator for its Goa facility.The...
Zydus Cadila gets USFDA nod to market antidepressant drug Ruby Khatun Khatun10 Oct 2017 10:30 AM ISTNew Delhi: Drug firm Zydus Cadila has received final approval from the US health regulator to market Amitriptyline hydrochloride tablets used for the...
Amazon is headed for the prescription-drug market, analysts say Ruby Khatun Khatun10 Oct 2017 10:01 AM ISTAmazon.com Inc. is almost certain to enter the business of selling prescription drugs by 2019, said two analysts at Leerink Partners, posing a direct...
HC asks Centre, Maharashtra to list steps taken to regulate online medicine sale Ruby Khatun Khatun9 Oct 2017 12:38 PM ISTMUMBAI: Expressing concern over the rampant unauthorized sale of medicines online, the Bombay High Court has asked the Maharashtra government and the...
Shilpa Medicare gets EIR from USFDA for Jadcherla facility Ruby Khatun Khatun9 Oct 2017 10:44 AM ISTNew Delhi: Shilpa Medicare on Saturday said the USFDA has issued an Establishment Inspection Report (EIR) for its Jadcherla facility in Telangana.The...
FDA awards 15 grants for clinical trials to stimulate product development for rare diseases Ruby Khatun Khatun9 Oct 2017 9:47 AM ISTThe U.S. Food and Drug Administration (FDA) announced that it has awarded 15 new clinical trial research grants totaling more than $22 million over...
Bayer sticks by Xarelto sales estimate despite study setback Ruby Khatun Khatun9 Oct 2017 9:20 AM ISTFRANKFURT/BERLIN: Bayer stood by its peak sales estimate for clot prevention drug Xarelto after the pill disappointed in a late-stage trial to test...
Why shift in drug pricing policy: SC asks Centre Ruby Khatun Khatun8 Oct 2017 12:06 PM ISTNew Delhi: A bench of Supreme Court headed by Chief Justice Dipak Misra, Justice A.M. Khanwilkar and Justice D.Y. Chandrachud recently asked the...
FDA approves first test for screening Zika virus in blood donations Ruby Khatun Khatun8 Oct 2017 10:15 AM ISTThe U.S. Food and Drug Administration approved the cobas Zika test, a qualitative nucleic acid test for the detection of Zika virus RNA in individual...
Granules India gets EIR from USFDA for Vizag OmniChem facility Ruby Khatun Khatun8 Oct 2017 10:01 AM ISTNew Delhi: Drug firm Granules India said it has received Establishment Inspection Report (EIR) from the US health regulator for the OmniChem facility...
Johnson and Johnson unit exits insulin pump business amid rising competition Ruby Khatun Khatun8 Oct 2017 10:00 AM ISTJohnson and Johnson’s diabetes care unit, which makes insulin pumps, said on Thursday it would shut its business in the United States and Canada amid...
At least six funds interested in Sanofi European generic drugs unit -Le Figaro Ruby Khatun Khatun8 Oct 2017 9:45 AM ISTPARIS: French pharmaceutical group Sanofi is set to start the process to sell its generic drug business in Europe, and at least six funds have...
