JOSÉ MORA - Eventura

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

Duration: 60 Minutes

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

Duration: 90 Minutes

21 CFR Part 820 - simplified controlled Documents Management

Duration: 90 Minutes

Test Method Validation to Verify your Device Performance

Duration: 60 Minutes

CAPA - utilizing the Principles of Lean Documents and Lean Configuration

Duration: 90 Minutes

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

Duration: 90 Minutes

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

Effective Design of Experiments (DOE) Strategies

Duration: 60 Minutes

FDA Regulations and Requirements for Artificial Intelligence / Machine Learning

Duration: 90 Minutes

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

Duration: 90 Minutes

Supplier Quality Management Simplified

Duration: 90 Minutes

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

Duration: 3 Hour

Demystifying Design Inputs - Design Outputs, Traceability Matrix

Duration: 90 Minutes

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

Duration: 90 Minutes

The FDA Inspection From SOP To 483

Duration: 90 Minutes

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

Seminar Completed | Recording and Pre-Registration Available

Sampling Plans for Verification, Validation and Production

Duration: 90 Minutes

FDA Labeling and UDI Essentials for Medical Products

Duration: 90 Minutes

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

_______________________________________________________________________________________________________ 📅 September 23, 2026 | 🕒 11 PM Eastern Time US | 🕒 3 PM GMT | ⏳ 90 Minutes

Maintaining Traceability Between User Requirements, Risk Controls and Verification Evidence

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

EU MDR Technical Documentation: Keeping Risk, Clinical and Design Records Consistent Through Product Changes

_______________________________________________________________________________________________________ 📅 September 14, 2026 | 🕒 11 PM Eastern Time US | 🕒 3 PM GMT | ⏳ 90 Minutes