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The Role of Medical Certifications in Ensuring Product Quality and Safety

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Product safety and quality in the healthcare sector are not options. Launching new medical devices, medicines, or diagnostic tools onto the market comes with rigorous validation to guarantee that they are safe and will deliver what they have to do to patients. Medical certifications are part of the process of validation to ensure products have undergone examined processes by experts and comply with international standards.

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Essential Details to Keep In Mind before Importing and Selling Medical Devices

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In a bid to improve the health sector, most governments and private parties import medical devices. However, it is not a “one call settles it all” kind of scenario. Depending on factors such as the prevailing market, international relations, foreign trade policies, your home country’s GDP, and the current regulations, the entire process can be a bit overwhelming.

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FDA Sweeps Aside Regulatory Barriers to Speed Production of Crucial Medical Products, Including Ventilators

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Washington DC, the U.S. Food and Drug Administration took significant action to help increase the availability of ventilators and accessories, as well as other respiratory devices, during the COVID-19 pandemic to support patients with respiratory failure or difficulty breathing.

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