Wednesday, November 9, 2022

CDSCO Import License for Medical Devices In India

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  Central Drugs Standard Control Organisation is, known as CDSCO, is a regulatory body for the Indian medical devices industry, under the vi...
Thursday, October 20, 2022

SFDA Medical device Registration & regulations

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  Saudi Arabia is evolving as growing market for healthcare sector, there are huge opportunities which are attracting to medical device manu...
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FDA 510K Submission & Certification for Saudi Arabia

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  Determining whether you need FDA 510k or PMA for your medical device will depend on the classification of your device. Every device manuf...
Saturday, October 8, 2022

 In Vitro Diagnostic Medical Device Regulation  

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  IVDR stands for In Vitro Diagnostic Regulation. IVDR is a risk-based approach to classify device with increased notified body and compet...
Tuesday, October 4, 2022

CE Marking Certification for Medical Devices.

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  CE certification is required for medical devices to demonstrate that your medical device meets the requirements of the Medical Device man...

 In Vitro Diagnostic Medical Device Regulation  

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IVDR stands for In Vitro Diagnostic Regulation . IVDR is a risk-based approach to classify device with increased notified body and compete...
Monday, August 22, 2022

Medical Device Regulatory Consultants

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  Medical device consultancies or the regulatory consultants are highly experienced professionals from healthcare industries. With rapid pos...