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      JOSÉ MORA


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      Recording

      Pharmaceutical Quality Management System – Applying the Principles of Lean Documents and Lean Configuration

      Duration: 60 Minutes

      JOSÉ MORA
      FDB1047
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      Recording

      ISO 13485:2016 using Lean Principles – Don’t let the New Requirements Surprise You

      Duration: 90 Minutes

      JOSÉ MORA
      MD1489
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      Recording

      21 CFR Part 820 - simplified controlled Documents Management

      Duration: 90 Minutes

      JOSÉ MORA
      MD1482
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      Recording

      Test Method Validation to Verify your Device Performance

      Duration: 60 Minutes

      JOSÉ MORA
      MD3048
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      Recording

      CAPA - utilizing the Principles of Lean Documents and Lean Configuration

      Duration: 90 Minutes

      JOSÉ MORA
      MD1480
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      Recording

      Advanced Course on Lean Documents, Lean Configuration and Document Control for Medical Devices

      Duration: 90 Minutes

      JOSÉ MORA
      MD1481
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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

      Duration: 90 Minutes

      JOSÉ MORA
      MD1942
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      Recording

      Effective Design of Experiments (DOE) Strategies

      Duration: 60 Minutes

      JOSÉ MORA
      MD3357
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      Recording

      FDA Regulations and Requirements for Artificial Intelligence / Machine Learning

      Duration: 90 Minutes

      JOSÉ MORA
      FDB3356
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      Recording

      Risk Management using Lean – Are you sure your documents are clutter free?

      Duration: 90 Minutes

      JOSÉ MORA
      MD3352
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      Recording

      Supplier Quality Management Simplified

      Duration: 90 Minutes

      JOSÉ MORA
      MD1945
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      Recording

      3-Hour Virtual Seminar on IEC 62304 and Demystifying Software Validation using the Principles of LDLC

      Duration: 3 Hour

      JOSÉ MORA
      MD3481
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      Recording

      Demystifying Design Inputs - Design Outputs, Traceability Matrix

      Duration: 90 Minutes

      JOSÉ MORA
      MD3044
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      Recording

      Sampling Plans For Verification And Validation, Production Process Validation And Production Control

      Duration: 90 Minutes

      JOSÉ MORA
      MD1887
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      Recording

      The FDA Inspection From SOP To 483

      Duration: 90 Minutes

      JOSÉ MORA
      FDB1888
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      Recording

      Process Validation Requirements and Compliance Strategies (Now in Spanish and English)

      Seminar Completed | Recording and Pre-Registration Available

      JOSÉ MORA
      MD3046
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      Recording

      Sampling Plans for Verification, Validation and Production

      Duration: 90 Minutes

      JOSÉ MORA
      FDB2287
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      Recording

      FDA Labeling and UDI Essentials for Medical Products

      Duration: 90 Minutes

      JOSÉ MORA
      MD2286
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      Live - AUG 18

      QMSR Device Records: Structuring DDF, MDF and Related Relationships for Inspection Readiness

      _______________________________________________________________________________________________________ 📅 August 18, 2026 | 🕒 11 PM Eastern Time US | 🕒 3 PM GMT | ⏳ 90 Minutes

      JOSÉ MORA
      MD1382
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      Live - AUG 31

      Configuration Control vs. Document Control – Managing Design Changes Across Modern Quality Systems

      _______________________________________________________________________________________________________ 📅 August 31, 2026 | 🕒 11 PM Eastern Time US | 🕒 3 PM GMT | ⏳ 90 Minutes

      JOSÉ MORA
      MD1383
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