Search For "drug administration"
Israeli startup's personalised cell therapy gets FDA fast-track designatio
Updated : 1 year, 2 months ago IST
Netanya-based biotechnology startup BioGenCell announced it has received the US Food and Drug Administration's Fast Track Designation for BGC101, a personalized cell therapy for severe Critical Limb Threatening Ischemia (CLTI).
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FDA Approves IMULDOSA® (ustekinumab-srlf), Accord BioPharma's Biosimi
Updated : 1 year, 5 months ago IST
Ahmedabad (Gujarat) [India], October 14: Accord BioPharma, Inc., the U.S. specialty division of Intas Pharmaceuticals, Ltd., focused on the development of oncology, immunology, and critical care therapies, announced that the U.S. Food and Drug Administration (FDA) has approved IMULDOSA (uste
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Lawmakers express concerns over US pharma companies' involvement in clinic
Updated : 1 year, 6 months ago IST
Several lawmakers have urged the US Food and Drug Administration to initiate an investigation over US biopharmaceutical companies conducting clinical trials alongside the People's Liberation Army (PLA) in Xinjiang, a press release by The Select Committee on the Chinese Communist Party (SCCCP
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Chilli powder imported from China seized at Taiwan border for pesticide re
Updated : 1 year, 7 months ago IST
Two shipments of chilli powder, amounting to 1,000 kilogrammes, imported by a Taiwan-based restaurant group from China were intercepted at Taiwan's border due to pesticide residue, the Central News Agency (CNA) reported, quoting the Food and Drug Administration (TFDA).
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Atul Bioscience Ltd Received EIR from the US FDA for its Ambernath Facilit
Updated : 1 year, 7 months ago IST
Mumbai (Maharashtra) [India], August 12: Atul Bioscience Ltd (ABL), a 100 per cent subsidiary company of Atul Ltd, received Establishment Inspection Report (EIR) from the United States Food and Drug Administration (US FDA) for its manufacturing facility situated in Ambernath, Maharashtra.
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Rusan Pharma's API Plant in Ankleshwar Receives (India) USFDA GMP Approval
Updated : 1 year, 7 months ago IST
Ankleshwar (Gujarat) [India], July 22: RUSAN PHARMA PRIVATE LIMITED, a pharmaceutical company based in India specializing in the area of addiction treatment and pain management, recently announced that the United States Food and Drug Administration (USFDA) has granted Good Manufacturing Prac
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Maharashtra: FDA conducts raids at three different locations in Vasai, sei
Updated : 1 year, 8 months ago IST
Food and Drug Administration (FDA) Maharashtra conducted raids at three different locations at Vasai on Thursday and found that a Pharma Products Pvt. Limited company was manufacturing drugs without obtaining licence for manufacturing of drugs at this place.
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US FDA inspection closed at its Injectable Facility with Zero 483 observat
Updated : 1 year, 9 months ago IST
According to the stock market filing with the National Stock Exchange, the U.S. FDA carried out the inspection between June 10 to June 13, 2024, and concluded with zero 483 observations. The pharma major said in its filing, "The United States Food and Drug Administration (U.S. FDA) has compl
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Uttarakhand: Hi-tech lab inaugurated to test medicines, medical equipment
Updated : 1 year, 9 months ago IST
On the instructions of Uttarakhand Chief Minister Pushkar Singh Dhami, a hi-tech lab has been inaugurated in Dehradun by the State Food Safety and Drug Administration Department to test medicines, medical equipment and cosmetic samples. In this lab, samples are being tested with state-of-the
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RNT Health Insights Private Limited Receives FDA Breakthrough Device Desig
Updated : 1 year, 9 months ago IST
Chandigarh [India], May 31: RNT Health Insights Private Limited, a clinical stage medical diagnostics company, is pleased to announce that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device Designation for their Early Gastric Cancer detection tool. Their innovative s
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Cipla secures USFDA approval for pancreatic disease injection, shares surg
Updated : 1 year, 9 months ago IST
Mumbai-headquartered pharma major, Cipla's US arm has secured final approval from the United States Food and Drug Administration (USFDA) for its Lanreotide Injection 120 mg/0.5 mL, 90 mg/0.3 mL, and 60 mg/0.2 mL.
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Biocon Biologics gets U.S. FDA approval for biosimilar aflibercept Yesafil
Updated : 1 year, 9 months ago IST
Biocon Biologics announced that the U.S. Food and Drug Administration (US FDA) has approved the company's application for YESAFILI, the company informed the exchange in a filing.
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