MEDTRONIC VASCULAR GALWAY UNLIMITED COMPANY
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Founded
1989-12-19
Website
Risk Signals
4962 news mentions monitored
Industry Context
This company is tracked across risk categories, including those related to its sector (e.g., Surgical and Medical Instruments and Apparatus, Drugs, Drug Proprietaries, and Druggists' Sundries), including supply chain integrity, ESG practices, labor disputes, and regulatory compliance.
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Recent Articles about MEDTRONIC VASCULAR GALWAY UNLIMITED COMPANY
Live alerts from global media, monitored by Business Radar
2025-03-01 (cardiovascularbusiness.com)
Week in Review: Pacemakers recalled | FDA ends semaglutide shortage | Researchers target Lp(a) | Comparing popular TAVR valves | Cardiovascular Business
The paclitaxel-coated device, already approved in Europe and other parts of the world, will be tested on more than 1,200 patients for a new international trial. If the study is a success, Medtronic hopes to gain regulatory approval in the United States and Japan.
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2025-02-28 (cardiovascularbusiness.com)
Comparing popular TAVR valves | Teleflex to acquire Biotronik assets for $791M | FDA sued over semaglutide | Google's good news | Cardiovascular Business
The paclitaxel-coated device, already approved in Europe and other parts of the world, will be tested on more than 1,200 patients for a new international trial. If the study is a success, Medtronic hopes to gain regulatory approval in the United States and Japan.
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2025-01-11 (pharmatutor.org)
Require Regulatory Affairs Specialist at Medtronic - M.Pharm, B.Pharm Apply |
He, she participates in all activities relating to preparation, submission and follow up to obtain approvals, renewals for products and its variations and line extension indications and labeling approvals of medical devices of various business units of Medtronic. He, she will be responsible for providing technical support by interpreting federal and local regulations as they apply to products, processes, practices and procedures
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2024-11-09 (pharmatutor.org)
Regulatory Affairs Specialist Require at Medtronic
Represent Regulatory Affairs as team member of product development projects from Concept through Commercialization. Review pre-clinical, and clinical protocols and associated reports to be used in submissions for assigned projects.
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2024-10-08 (pharmatutor.org)
Regulatory Affairs Specialist Require at Medtronic
Represent Regulatory Affairs as team member of product development projects from Concept through Commercialization. Review pre-clinical, and clinical protocols and associated reports to be used in submissions for assigned projects.
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2024-09-16 (macaubusiness.com)
China’s service trade fair facilitates medical business
China, MNA | A wireless pacemaker that is only the size of a capsule attracted exhibitors and visitors at the ongoing 2024 China International Fair for Trade in Services (CIFTIS).
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2023-08-23 (kfgo.com)
US FDA panel votes against use of Medtronic’s blood pressure treatment device
(Reuters) -The U.S. Food and Drug Administration's independent experts on Wednesday narrowly voted against recommending the approval of Medtronic's blood pressure treatment device, saying risks tied to using it do not outweigh the benefits. The same pa...
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2010-02-02 (informa.com)
Medtronic's "tremendous" transcatheter heart valve reaches the US – UPDATE
The US FDA has approved Medtronic's transcatheter pulmonary heart valve, Melody, under a humanitarian device exemption (HDE).
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(ryortho.com)
Medtronic Opens Chinese Innovation Center
Medtronic, Inc. has officially opened an Innovation Center in Shanghai, China. In an August 27 announcement, the company said the new facility, located in the company’ s China headquarters and the first outside the U.S. and Europe, `` represents the company 's initial step in creating local
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