HUNGARY | Updated ETT-TUKEB Medical Device Procedures
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CROATIA | Updated CEC Submission Requirements
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LITHUANIA | Updated LBEK Submission Requirements for Medical Devices
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UK | Revised Reporting Requirements for Non-CTIMPs
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AUSTRALIA | Updated Requirements for Post-Marketing Surveillance Studies
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USA | New eCFR Website
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BULGARIA | New Version of the ECKI NIS SOP
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EU | HMA-EMA Big Data Steering Group 2021 – 2023 Workplan
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SPAIN | AEMPS Updates – Relevant to ICFs
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