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A Practical Approach to Medical Device Risk Management
$249.00
Harvey Rudolph
Avoiding FDA 483s, Warning Letters and Recalls with Harmonized Supplier Qualification
$249.00
John Avellanet
Correction and CAPA: What's the Difference?
$249.00
Dan O'Leary
Device Master Records & Device History Records: Are You Compliant?
$249.00
Dan O'Leary
Driving Your Quality System With Effective Management Controls
$249.00
Vinny Sastri
Establishing an Effective Quality Management System: Benchmark Leading Practices
$249.00
Bill Hoover & Noel Sobelman
Excel Spreadsheets and FDA Medical Device Regulations
$249.00
Dan O'Leary
Failure Modes & Effects Analysis (FMEA)
$249.00
Angelo Scangas
Generating Risk-Based Design Input Early in the Design Process
$249.00
Bernard Bosley
How to Successfully Execute an FDA Product Recall
$249.00
Bruce MacFarlane
Managing the Medical Device Supply Chain
$249.00
Dan O'Leary
Post-Marketing Issues for Medical Device Companies
$249.00
Caryn Silverman
Process and SOP Development for Medical Device Companies
$249.00
Phil Guarino
Process Validation for Medical Devices
$249.00
Dan O'Leary
Regulatory Requirements for Medical Device Calibration Programs
$249.00
Dan O'Leary
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