Eventura World
Eventura World
Courses
Blogs
Eventura World
Eventura World
Courses
Blogs
Courses #seminar
Writing Validation Master Plans – Best Practices for Writing a Compliant Document
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Analytical Instrument Qualification & Validation - Use of Excel and FDA Audit Preparation
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Production and Process Controls for Medical Devices
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EU's New Regulation 535/2014 On Clinical Trials - Insights Into Effective Clinical Trials
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Risk Management for ML Medical Devices following AAMI/ BSI TR 34971 and ISO 14971
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Good Clinical Practices Review of ICH E6 (R3) Latest Guidance
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Continued Process Verification and Process Monitoring
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Human Error Investigation Program - Effective Implementation
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FDA/ICH Guideline Q9 (R1) On Quality Risk Management
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3-Hour Virtual Seminar On IEC 62304 - Medical Device Software Compliance
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Death by CAPA - Does your CAPA Program need a CAPA?
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The DHF, Technical Documentation - Similarities, Differences and the Future
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