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TRAINING WHITE PAPERS
Coaching to Improve Training ResultsDo You Need a Trainer or a Training Consultant
Benefits of e-LearningHow to Source Training
The Advantages of Certifying In-House TrainersIs our Subject Matter Expert (SME) the right choice to become our in-house trainer?
The Unlocked Potential of your Training ResourcescGMP Annual Training
To Train or Not to Train? In a Regulatory Inspection, How do you Justify Training?
Qualification of Key RolesImplementing a Competency Based Training System
The Importance of Role Based TrainingWhat is Human Error and Strategies for Addressing It?
Identifying and Overcoming Human Error

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Self-paced online e-learning modules include:

Combination Products

biologic pathogen

Biologics

Good Documentation Practices

Introduction to Change Control

Intro to Human Factors & Performance

Introduction to Technical Writing

Electronic Records & Signatures

Introduction to Quality Risk Management

Inspection Readiness

Good Clinical Practices

Current Good Manufacturing Practices

Intro to CAPA

Effective Meetings

ISO 13485

EU MDR 2017/795

Quality System Regulation

On-Demand Webinar titles include:

Defining Training in the Life Science Industry

Human Error is Not a Root Cause

Do Your SOPs Need a CAPA Investigation

Why the FMEA is Not Your Risk Management System

Conducting Third Party Audits

How to Document Quality Investigations

Changes and Updates to ISO 14971:2019

Building A Culture of Quality

Implementation & Management of GMP Data Integrity

Assessment Tools for Better Writing

Quality System Management Effectiveness

How to Qualify Lead Investigators for CAPA