MEREDITH CRABTREE - Eventura

FDA/ICH Guideline Q9 (R1) On Quality Risk Management

Duration: 90 Minutes

MEREDITH CRABTREE

3-Hour Virtual Seminar On Root Cause Analysis, CAPA And Effectiveness Checks

Duration: 3 Hour

MEREDITH CRABTREE

Latest Regulations For Quality Metrics And KPIS

Duration: 90 Minutes

MEREDITH CRABTREE

Preventive Maintenance And Calibrations - Regulatory Expectations And Best Practices

Duration: 90 Minutes

MEREDITH CRABTREE

FDA Regulation For Over-The-Counter (OTC) Drug Products

Duration: 90 Minutes

MEREDITH CRABTREE

Conducting Successful Complaint Investigations In Regulated Industries

Duration: 90 Minutes

MEREDITH CRABTREE

Effective Internal Audit Program

2-Day Seminar Completed | Recording and Pre-Registration Available

MEREDITH CRABTREE

FDA Warning Letter - Consent Decree Software Validation

Duration: 90 Minutes

MEREDITH CRABTREE

Performance of Root Cause Analysis, CAPA, and Effectiveness Checks

March 27 - 28, 2025 | US Eastern Time: 9 AM to 2 PM | Central Europe Time: 3 PM to 8 PM

MEREDITH CRABTREE

Aseptic Processing and Validation Course - FDA Expectations and Industry Best Practices

October 27 - 28, 2025 | US Eastern Time: 9 AM to 2 PM | Central Europe Time: 2 PM to 7 PM

MEREDITH CRABTREE

OOS and OOT Investigations Course - Best Practices, Key Components and FDA Requirements

Course Available for Immediate Viewing Total Duration: 9 Hours

MEREDITH CRABTREE

Aseptic Processing and Contamination Control Under EU GMP Annex 1: Practical Applications for Modern Sterile Operations

_______________________________________________________________________________________________________ Instant Streaming Available | 90 Minutes Learning Time

MEREDITH CRABTREE

Analytical Lifecycle Management Under ICH Q14 and Q2(R2): What Changes Operationally

_______________________________________________________________________________________________________ 📅 August 21, 2026 | 🕒 11 AM Eastern Time US | 🕒 3 PM GMT | ⏳ 90 Minutes

MEREDITH CRABTREE