What Regulations Apply To Medical Device Packaging?
When you manufacture, import or purchase medical devices, have you ever focused on their functionality, design, or the technology they use? Do
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When you manufacture, import or purchase medical devices, have you ever focused on their functionality, design, or the technology they use? Do
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In the global world of medical devices, packaging plays a major role in making sure that the safety and effectiveness of the
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Imagine your medical test results that are wrong. It could to misdiagnosis, delayed treatment, or unnecessary stress. So to avoid all these
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Imagine you are running a business where every tiny detail matters – If YES you must understand “How safely products are made
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ISO 13485 is an international standard identifying the need for a quality management system (QMS) specifically for the medical device industry. It
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ISO standards play an essential role in the medical device industry by ensuring that all the products are safe, reliable, and fulfil
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ISO 13485 is the quality management system that maintains the quality of medical devices in India. So, if you are dealing with
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Navigating the landscape of medical regulation can be haunting, especially for those interested in self-testing IVD diagnostics in India. The interval of
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When you are a manufacturer, importer or wholesaler of medical devices then you must understand the licensing process. It includes licenses of
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If you are an importer and you want to Import medical devices into India, then both Form MD-26 and MD-27 are important
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