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November 26, 2025 04:04 ET | Source: Research and Markets

2 Day Efficient Batch Record Design and Review Training Course (Online Event: Dec 10th - Dec 11th, 2025)

Dublin, Nov. 26, 2025 (GLOBE NEWSWIRE) -- The "Efficient Batch Record Design and Review Training (Online Course) (Dec 10th - Dec 11th, 2025)" training has been added to ResearchAndMarkets.com's...
November 05, 2025 10:49 ET | Source: Research and Markets

Pharma 4.0 Focus Data Integrity by Design Training Webinar: Newer Approaches and Technologies to Cost Effective 21 CFR Part 11 Compliance

Dublin, Nov. 05, 2025 (GLOBE NEWSWIRE) -- The "Pharma 4.0 Focus Data Integrity by Design - Newer Approaches and Technologies to Cost Effective 21 CFR Part 11 Compliance (Aug 19, 2025)" training has...
July 17, 2025 04:04 ET | Source: Research and Markets

From Issuance to Final QA | Efficient Batch Record Design and Review Training Course (ONLINE EVENT: September 9-10, 2025)

Dublin, July 17, 2025 (GLOBE NEWSWIRE) -- The "Efficient Batch Record Design and Review Training" training has been added to ResearchAndMarkets.com's offering. This online training is designed for...
May 14, 2025 08:21 ET | Source: Research and Markets

Master Risk-Based Computer System Validation to Cut Implementation Time - 2 Day Online Course (August 6-7, 2025) | Essential Training for GxP Professionals in Health Care and Biopharma Sectors

Dublin, May 14, 2025 (GLOBE NEWSWIRE) -- The "Risk-based Computer System Validation; Reduce Costs and Avoid 483s (ONLINE EVENT: August 6-7, 2025)" has been added to ResearchAndMarkets.com's...
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...
December 04, 2024 04:49 ET | Source: Research and Markets

21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries Webinar (ONLINE EVENT: December 18, 2024/ON-DEMAND)

Dublin, Dec. 04, 2024 (GLOBE NEWSWIRE) -- The "21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries" webinar has been added to ...
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...
May 30, 2023 06:38 ET | Source: Research and Markets

21 CFR Part 11 Compliance for Computer Systems Regulated by FDA - 6-Hour Virtual Seminar

Dublin, May 30, 2023 (GLOBE NEWSWIRE) -- The "6-Hour Virtual Seminar on 21 CFR Part 11 Compliance for Computer Systems Regulated by FDA" webinar has been added to ResearchAndMarkets.com's...
April 20, 2023 08:13 ET | Source: Research and Markets

3 Day Computer System Validation ( CSV) Virtual Course

Dublin, April 20, 2023 (GLOBE NEWSWIRE) -- The "Computer System Validation ( CSV) 3 Day Virtual Seminar" training has been added to ResearchAndMarkets.com's offering. This course is designed to...
October 07, 2022 04:08 ET | Source: Research and Markets

3 Day Computer System Validation (CSV) Virtual Seminar: October 31, 2022 - November 2, 2022

Dublin, Oct. 07, 2022 (GLOBE NEWSWIRE) -- The "Computer System Validation ( CSV) 3 Day Virtual Seminar" training has been added to ResearchAndMarkets.com's offering. This course is designed to...