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JOSÉ MORA
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Recording
Pharmaceutical Quality Management System – Applying the Principles of Lean Documents and Lean Configuration
FDB1047
JOSÉ MORA
Duration: 60 Minutes
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Recording
ISO 13485:2016 using Lean Principles – Don’t let the New Requirements Surprise You
MD1489
JOSÉ MORA
Duration: 90 Minutes
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Recording
21 CFR Part 820 - simplified controlled Documents Management
MD1482
JOSÉ MORA
Duration: 90 Minutes
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Recording
Test Method Validation to Verify your Device Performance
MD3048
JOSÉ MORA
Duration: 60 Minutes
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Recording
CAPA - utilizing the Principles of Lean Documents and Lean Configuration
MD1480
JOSÉ MORA
Duration: 90 Minutes
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Recording
Advanced Course on Lean Documents, Lean Configuration and Document Control for Medical Devices
MD1481
JOSÉ MORA
Duration: 90 Minutes
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Recording
Creating Design History Files (DHF), the Device Master Records (DMR) and the Device History Records (DHR), Utilizing the Principles of Lean Documents and Lean Configuration
MD1942
JOSÉ MORA
Duration: 90 Minutes
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Recording
Effective Design of Experiments (DOE) Strategies
MD3357
JOSÉ MORA
Duration: 60 Minutes
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Recording
FDA Regulations and Requirements for Artificial Intelligence / Machine Learning
FDB3356
JOSÉ MORA
Duration: 90 Minutes
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Recording
Risk Management using Lean – Are you sure your documents are clutter free?
MD3352
JOSÉ MORA
Duration: 90 Minutes
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Recording
Supplier Quality Management Simplified
MD1945
JOSÉ MORA
Duration: 90 Minutes
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Recording
Process Validation Requirements and Compliance Strategies
MD3046
JOSÉ MORA
Duration: 60 Minutes
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Recording
3-Hour Virtual Seminar on IEC 62304 and Demystifying Software Validation using the Principles of LDLC
MD3481
JOSÉ MORA
Duration: 3 Hour
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Recording
Demystifying Design Inputs - Design Outputs, Traceability Matrix
MD3044
JOSÉ MORA
Duration: 90 Minutes
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