MEREDITH CRABTREE

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Recording
  

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

FDB3610
MEREDITH CRABTREE

Duration: 90 Minutes

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Recording
  

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

FDB3611
MEREDITH CRABTREE

Duration: 3 Hour

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Recording
  

Latest Regulations For Quality Metrics And KPIS

FDB3615
MEREDITH CRABTREE

Duration: 90 Minutes

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Recording
  

Preventive Maintenance And Calibrations - Regulatory Expectations And Best Practices

FDB3613
MEREDITH CRABTREE

Duration: 90 Minutes

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Recording
  

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

FDB3614
MEREDITH CRABTREE

Duration: 90 Minutes

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15 OCT '24
  

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

FDB3616
MEREDITH CRABTREE

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

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Recording
  

Conducting Successful Complaint Investigations In Regulated Industries

FDB3618
MEREDITH CRABTREE

Duration: 90 Minutes

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Recording
  

Effective Internal Audit Program

SEM3112
MEREDITH CRABTREE

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

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Recording
  

FDA Warning Letter - Consent Decree Software Validation

FDB3619
MEREDITH CRABTREE

Duration: 90 Minutes