Eventura World
Eventura World
Courses
Blogs
Eventura World
Eventura World
Courses
Blogs
Courses
ICH Q7 – GMPs for Active Pharmaceutical Ingredients
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3-Hour Virtual Seminar on Validation and Part 11 Compliance of Computer Systems
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COMPUTER SYSTEM VALIDATION FOR CLOUD AND COTS APPLICATIONS
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Artificial Intelligence in Pharmaceutical GMP Operations - Case Studies
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How to go Paperless in an FDA-Regulated Environment using Electronic Workflow Signature Approvals and Electronic Records
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OBJECTIONABLE MICROORGANISMS IN BIOPHARMACEUTICAL PRODUCTION – IDENTIFICATION AND RISK MITIGATION
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OOS Test Results – Latest FDA Guidance
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4-Hour Virtual Seminar on Project Management for Non-Project Managers
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DATA INTEGRITY BY DESIGN, PHARMA 4.0 AND OVERCOMING DI ISSUES IN THE CLOUD
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SDLC Modernization Continuous Quality in an FDA-Regulated Environment and Journey to Paperless SDLC/CSV
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Preventive Maintenance and Calibrations – Regulatory Expectations and Best Practices
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3-Hour Virtual Seminar on cGMP Regulatory Inspections – Through the Eyes of FDA, EMA and PMDA
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