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January 21, 2025 09:30 ET | Source: Research and Markets

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

Dublin, Jan. 21, 2025 (GLOBE NEWSWIRE) -- The "Efficient Batch Record Design and Review" training has been added to ResearchAndMarkets.com's offering. This accredited training will identify and...
September 30, 2024 06:11 ET | Source: Research and Markets

Efficient Batch Record Design and Review Course: Regulatory Requirements Applying to Batch Record Review, Pharmaceutical Documentation & the Quality System (ONLINE: November 11-13, 2024 / ON-DEMAND)

Dublin, Sept. 30, 2024 (GLOBE NEWSWIRE) -- The "Efficient Batch Record Design and Review" training has been added to ResearchAndMarkets.com's offering. This online training is designed for...
October 25, 2023 07:13 ET | Source: Research and Markets

Pharmaceutical Industry Advances in Regulatory Compliance: New 4-Hour Virtual Seminar Revealed in Light of Upcoming UK Government Deal

Dublin, Oct. 25, 2023 (GLOBE NEWSWIRE) -- The recent Financial Times revelation that the pharmaceutical industry is nearing an accord with the UK government over drug pricing has rippled through the...
June 12, 2023 07:33 ET | Source: Research and Markets

2023 Efficient Batch Record Review and Product Release Training - Webinar

Dublin, June 12, 2023 (GLOBE NEWSWIRE) -- The "Efficient Batch Record Review and Product Release Training" webinar has been added to ResearchAndMarkets.com's offering. Most Regulatory Agencies...
April 06, 2023 09:38 ET | Source: Research and Markets

The DHF, DMR, DHR, EU MDR Technical Documentation Similarities, Differences and The Future (April 28, 2023)

Dublin, April 06, 2023 (GLOBE NEWSWIRE) -- The "The DHF, DMR, DHR, EU MDR Technical Documentation Similarities, Differences and The Future" training has been added to ResearchAndMarkets.com's...