Search For "us fda"
Lord's Mark Becomes one of the Firm with 153 US FDA-Listed Products
Updated : 2 months, 2 weeks ago IST
New Delhi [India], January 8: Lord's Mark Industries Ltd, one of India's fastest-growing diversified conglomerates, has achieved a significant milestone by becoming one of the companies to secure US FDA registrations covering 153 orthosurgical products, setting a new benchmark for Indian med
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US: FDA flags several India manufactured cookware with possibility to leac
Updated : 3 months, 4 weeks ago IST
America's Food and Drug Administration (FDA) has warned consumers about 19 types of cookware, several of which are made in India out of aluminum and alloys that risk leaching of lead into food CBS reported on Thursday.
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Reghelps SRC Launches Specialized Clinical Investigation, PMCF, and IVD Pe
Updated : 5 months, 1 week ago IST
Bangalore (Karnataka) [India], October 14: Reghelps SRC, a newly established Contract Research Organization (CRO) in India, announced the launch of its comprehensive clinical research services for global Medical Device and In-Vitro Diagnostic Device (IVD) manufacturers.
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Central Consumer Protection Authority fines VLCC limited Rs 3 Lakh for mis
Updated : 7 months ago IST
The Central Consumer Protection Authority imposed a Rs 3 lakh penalty on VLCC for publishing misleading advertisements promoting CoolSculpting as a permanent weight-loss solution. CCPA emphasized that the US-FDA approved procedure is only for localized fat reduction in specific body areas
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President Lula welcomed Indian companies to manufacture drugs, pharmaceuti
Updated : 8 months, 2 weeks ago IST
During the MEA briefing, India's Ambassador to Brazil, Dinesh Bhatia, said that 15 large Indian laboratories and pharmaceutical companies are already present in Brazil, many of whom he said do manufacturing in the South American country.
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Nureca Limited's Manufacturing Subsidiary Secures US FDA Registration
Updated : 11 months, 2 weeks ago IST
Mumbai (Maharashtra) [India], April 12: Nureca Technologies Private Limited, the manufacturing subsidiary of Nureca Limited, has successfully completed its annual registration with the United States Food and Drug Administration (US FDA). The company's manufacturing facility in Mohali, Punjab
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RNT Health Insights Receives Second US FDA Breakthrough Device Designation
Updated : 1 year, 2 months ago IST
Chandigarh [India], January 9: RNT Health Insights, a Chandigarh-based health-tech startup specializing in AI-assisted diagnostic solutions for the accurate detection of pathologies during endoscopic procedures, has been granted its second US FDA Breakthrough Device Designation for its Esoph
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Israeli startup's personalised cell therapy gets FDA fast-track designatio
Updated : 1 year, 3 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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Hexaware Launches QCaaS in Partnership with Archimedis Digital
Updated : 1 year, 4 months ago IST
Mumbai (Maharashtra) [India], November 21: Hexaware Technologies, a provider of IT services and solutions, has partnered with Archimedis Digital to introduce Quality & Compliance as a Solution (QCaaS). Inspired by Computerized Systems Assurance (CSA) and powered by Artificial Intelligenc
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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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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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Biocon Biologics gets U.S. FDA approval for biosimilar aflibercept Yesafil
Updated : 1 year, 10 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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