AZAVAI learning paths

Progress through the quality decisions you need to master

Structured paths connect GxP fundamentals with professional situations that require a clear, traceable and defensible decision.

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4 parcours
FoundationsFoundation

GxP Foundations

Build a solid quality reasoning foundation by mastering GxP vocabulary, principles, and responsibilities from day one.

Target audienceNewcomers to GxP environments, professionals transitioning into quality, pharmaceutical science students.
3 courses3h
  1. 1Pilot course — GMP fundamentals and quality systemFoundation45 to 60 min
  2. 2GMP fundamentals and quality systemFoundation45 to 60 min
  3. 3Quality risk management according to ICH Q9Intermediate45 to 60 min
OperationsIntermediate

Operational Quality Mastery

Develop the reflexes to qualify deviations, protect data integrity, manage change, and apply the ICH Q10 quality system in daily operations.

Target audienceQuality operators, production technicians, deviation/CAPA leads, data integrity champions.
4 courses4h
  1. 1Data integrity and ALCOA+ in GxP environmentsIntermediate45 to 60 min
  2. 2Deviations, OOS and CAPAIntermediate45 to 60 min
  3. 3Change control and lifecycle managementIntermediate45 to 60 min
  4. 4Pharmaceutical quality system according to ICH Q10Intermediate45 to 60 min
LeadershipAdvanced

Quality Leadership & Inspection Readiness

Structure quality governance, prepare evidence of a controlled system, and qualify critical suppliers to face audits and inspections with confidence.

Target audienceQuality managers, QA directors, audit leads, qualified persons, regulatory affairs experts.
3 courses3h
  1. 1GMP audits and inspection readinessAdvanced45 to 60 min
  2. 2Supplier qualificationIntermediate45 to 60 min
  3. 3Responsible artificial intelligence in regulated pharmaceutical environmentsExploratory45 to 60 min
ValidationAdvanced

Validation & Qualification Expertise

Master the DQ/IQ/OQ/PQ articulation, design robust cleaning and process validation strategies that meet regulatory expectations.

Target audienceValidation engineers, qualification specialists, process owners, C&Q experts, GMP consultants.
3 courses3h
  1. 1Validation and qualification in GxP — DQ, IQ, OQ and PQIntermediate45 to 60 min
  2. 2Cleaning validationAdvanced45 to 60 min
  3. 3Process validationAdvanced45 to 60 min
Contact AZAVAI to ask about learning-path availability and support options.