Curriculum

Quality Management Systems

A quality management system (QMS) in the life sciences industry is a comprehensive framework designed to ensure that products and services meet the highest quality standards. It involves a systematic approach to identifying, controlling, and continuously improving processes related to product development, manufacturing, distribution, and post-market surveillance. A QMS typically includes elements such as Document Control, Training, Risk Management, Change Control, Deviations, and Corrective and Preventive Actions. By implementing a robust QMS, life sciences organizations can minimize risks, enhance product quality, ensure regulatory compliance, and protect public health.

Good Documentation Practices (GDocP)

CAPA and Effectiveness Checks

Learn More

Supplier Quality Management

Supplier Quality Management

Learn More

International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)

ICH Q9 – Quality Risk Management

Learn More

FDA Inspection Readiness (GMP Auditing)

How Self-Inspection Leads to Continuous Improvement

Learn More

Good Manufacturing Practices (cGMP) - Beginner

What are CAPA’s?

Learn More

Good Manufacturing Practices (cGMP) - Beginner

What are Deviations?

Learn More

Courses

Browse our extensive catalog of GxP, Corporate Compliance and EH&S training.

Learning Strategy

Boost your organization’s training with LearnGxP’s Learning Strategy Consultants (LSC). They customize learning paths to match your needs, offering ongoing support for lasting success.

Customer Stories

Discover how LearnGxP addresses real challenges, provides effective solutions, and positively impacts our customers’ organizations.