Maven

Effective Risk Management Insights
and Resources

November 14th, 2024
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Good Documentation Practices (GDP)

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November 7th, 2024
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Understanding MDCG 2020-5 for Medical Device Equivalence

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October 31st, 2024
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How to Handle the Customer Complaints according to various regulatory frameworks?

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October 24th, 2024
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Overview Of ETO Sterilization For Medical Devices

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October 16th, 2024
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ARTICLE 61(10) OF REGULATION (EU) 2017/745

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October 10th, 2024
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MDCG 2020-7 PMCF Plan Template: A Guide For Manufacturers And Notified Bodies

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October 3rd, 2024
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Medical Devices Manufactured Utilizing Tissues Or Cells Of Animal Origin

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September 25th, 2024
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Import License for Medical Devices from CDSCO

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September 16th, 2024
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CDSCO Manufacturing License for Medical Devices

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September 14th, 2024
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Importance of Clinical Data in EU MDR Compliance & Device Safety

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