MEREDITH CRABTREE - Eventura

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

MEREDITH CRABTREE

Duration: 90 Minutes

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

MEREDITH CRABTREE

Duration: 3 Hour

Latest Regulations For Quality Metrics And KPIS

MEREDITH CRABTREE

Duration: 90 Minutes

Preventive Maintenance And Calibrations - Regulatory Expectations And Best Practices

MEREDITH CRABTREE

Duration: 90 Minutes

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

MEREDITH CRABTREE

Duration: 90 Minutes

Is it a Drug, a Medical Device or both? Determine Product Classification with Precision and Risk

MEREDITH CRABTREE

October 15, 2024 | US Eastern Time: 9 AM to 3 PM | Central Europe Time: 3 PM to 9 PM

Conducting Successful Complaint Investigations In Regulated Industries

MEREDITH CRABTREE

Duration: 90 Minutes

Effective Internal Audit Program

MEREDITH CRABTREE

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

FDA Warning Letter - Consent Decree Software Validation

MEREDITH CRABTREE

Duration: 90 Minutes

Performance of Root Cause Analysis, CAPA, and Effectiveness Checks

MEREDITH CRABTREE

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

FDA Inspections - Top FDA 483 Observations and Prevention Strategies

MEREDITH CRABTREE

August 11 - 12, 2025 | US Eastern Time: 9 AM to 2 PM | Central Europe Time: 3 PM to 8 PM

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

MEREDITH CRABTREE

October 20 - 21, 2025 | US Eastern Time: 9 AM to 2 PM | Central Europe Time: 3 PM to 8 PM

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

MEREDITH CRABTREE

September 04 - 05, 2025 | US Eastern Time: 9 AM to 2 PM | Central Europe Time: 3 PM to 8 PM