Eventura World us
Eventura World
Courses
Blogs
Eventura World us
Eventura World
Courses
Blogs
Courses #Virtual Seminar
Good Manufacturing Practices (GMP) 101
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FDA Inspections Seminar for 2024
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Developing Effective Post Market Surveillance and Complaint Handling Requirements (Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls)
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Design of Experiments 101 - Methods and Analysis
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3 Hours Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries
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3-HOUR CERTIFICATION COURSE ON GOOD MANUFACTURING PRACTICES (GMP) – AN INTRODUCTION
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3-Hour Virtual Seminar On Root Cause Analysis, CAPA And Effectiveness Checks
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3-Hour Virtual Seminar on Bad Standard Operating Procedures (SOPs) – Bad Training: Garbage In, Garbage Out
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3-Hour Virtual Seminar on Master Validation Plan – The Unwritten Requirements
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3-Hour Virtual Seminar on Effective Cleaning Validation Procedures – Best Practices
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3-Hour Virtual Seminar on Successful Deviation Investigations
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3-Hour Virtual Seminar on Complaint Handling and Medical Device Reporting and Recalls
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