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Master Clinical Evidence for Medical Devices: Register for the Online Training on Regulatory Compliance & Post-Market Studies (April 7-8, 2025)
Dublin, Feb. 05, 2025 (GLOBE NEWSWIRE) -- The "Medical Device Studies: Clinical Evidence Training Course (ONLINE EVENT: April 7-8, 2025)" has been added to ResearchAndMarkets.com's offering.
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Virtual Efficient Batch Record Design and Review Course: Master Batch Records (MBR), Regulatory Requirements, Key Steps for Issuance, Reconciliation, and Final QA Disposition ...
This accredited training will identify and discuss Master Batch Records (MBR), regulatory ... for professionals in the Pharmaceutical, Medical Device, and other life science industries.