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Dublin, March 19, 2025 (GLOBE NEWSWIRE) -- The "FDA Inspection Preparedness and Compliance (ONLINE EVENT: May 7-8, 2025)" training seminar has been added to ResearchAndMarkets.com's offering. ...
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FDA Inspection Seminar: Preparations for Pharmaceutical and Medical Device Professionals (ON-DEMAND)
Dublin, March 10, 2025 (GLOBE NEWSWIRE) -- The "FDA Inspection" training has been added to ResearchAndMarkets.com's offering. This seminar provides the fundamentals and the ground rules on how to...
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Dublin, Feb. 17, 2025 (GLOBE NEWSWIRE) -- The "Best Practice for Writing Effective SOPs (Standard Operating Procedures) Training Course" conference has been added to ResearchAndMarkets.com's...
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Egnyte and Espero Partner to Deliver Intelligent, AI-Powered Solutions for Clinical Trial Management
Egnyte and Espero are announcing a strategic partnership that combines their artificial intelligence capabilities to revolutionize clinical trials.
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Dublin, Jan. 30, 2025 (GLOBE NEWSWIRE) -- The "FDA Inspections: From Site Preparation to Response" training has been added to ResearchAndMarkets.com's offering. This is a practical, hands-on...
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Dublin, Nov. 11, 2024 (GLOBE NEWSWIRE) -- The "Best Practice for Writing Effective SOPs (Standard Operating Procedures) Training Course" conference has been added to ResearchAndMarkets.com's...
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Dublin, Nov. 08, 2024 (GLOBE NEWSWIRE) -- The "FDA Inspection Preparedness and Compliance" training has been added to ResearchAndMarkets.com's offering. This is a practical, hands-on two-day...
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Blue Mountain announces the launch of Blue Mountain University, an eLearning platform for RAM software users to enhance skills, efficiency, and compliance.
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Dublin, Sept. 02, 2024 (GLOBE NEWSWIRE) -- The "FDA Inspection Preparedness and Compliance" training has been added to ResearchAndMarkets.com's offering. This is a practical, hands-on two-day...
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Dublin, Sept. 02, 2024 (GLOBE NEWSWIRE) -- The "FDA Inspection" training has been added to ResearchAndMarkets.com's offering. The course will go through what typically goes on during an FDA...