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Batch Record Review and Product Release Training Webinar: FDA 21 CFR 210/211 Expectations, Deviation Handling, CMO Oversight, and ICH Q10–ISO 13485 Alignment (ONLINE EVENT)

Dublin, Jan. 07, 2026 (GLOBE NEWSWIRE) -- The "Batch Record Review and Product Release (Jan 13, 2026)" training has been added to ResearchAndMarkets.com's offering. This course shows how to review ...
Business Wire

Virtual Efficient Batch Record Design and Review Course: Master Batch Records (MBR), Regulatory Requirements, Key Steps for Issuance, Reconciliation, and Final QA Disposition ...

DUBLIN--(BUSINESS WIRE)--The "Efficient Batch Record Design and Review" training has been added to ResearchAndMarkets.com's offering. This accredited training will identify and discuss Master Batch ...
Business Wire

Efficient Batch Record Design and Review Course: Regulatory Requirements Applying to Batch Record Review, Pharmaceutical Documentation & the Quality System (ONLINE: November 11 ...

DUBLIN--(BUSINESS WIRE)--The "Efficient Batch Record Design and Review" training has been added to ResearchAndMarkets.com's offering. This online training is designed for professionals in the ...
Mena FN

Batch Record Review And Product Release Training Webinar: FDA 21 CFR 210/211 Expectations, Deviation Handling, CMO Oversight, And ICH Q10ISO 13485 Alignment (ONLINE EVENT)

(MENAFN- GlobeNewsWire - Nasdaq) The main market opportunity lies in providing practical, inspection-ready training for batch record review tailored to pharma, biologics, and medical device fields. By ...