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November 14th, 2024
Maven
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Good Documentation Practices (GDP)
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November 7th, 2024
Maven
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Understanding MDCG 2020-5 for Medical Device Equivalence
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October 31st, 2024
Maven
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How to Handle the Customer Complaints according to various regulatory frameworks?
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October 24th, 2024
Maven
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Overview Of ETO Sterilization For Medical Devices
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October 16th, 2024
Maven
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ARTICLE 61(10) OF REGULATION (EU) 2017/745
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October 10th, 2024
Maven
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MDCG 2020-7 PMCF Plan Template: A Guide For Manufacturers And Notified Bodies
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October 3rd, 2024
Maven
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Medical Devices Manufactured Utilizing Tissues Or Cells Of Animal Origin
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September 25th, 2024
Maven
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Import License for Medical Devices from CDSCO
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September 16th, 2024
Maven
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CDSCO Manufacturing License for Medical Devices
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September 14th, 2024
Maven
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Importance of Clinical Data in EU MDR Compliance & Device Safety
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Recent Post
November 14th, 2024
Good Documentation Practices (GDP)
Read More
November 7th, 2024
Understanding MDCG 2020-5 for Medical Device Equivalence
Read More
October 31st, 2024
How to Handle the Customer Complaints according to various regulatory frameworks?
Read More