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

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

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

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

MEREDITH CRABTREE

📅 November 24, 2025 | 🕒 11 AM Eastern Time US | ⏳ 90 Minutes

Audit 101 - How to Conduct an Effective Audit & What They Don't Tell You May Happen

MEREDITH CRABTREE

📅 October 23, 2025 | 🕒 11 AM Eastern Time US | ⏳ 90 Minutes

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

MEREDITH CRABTREE

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