Regulated Industries • GMP Compliance • Data Integrity

GMP Training, Consultancy & Digital Quality Solutions

Practical, regulator-ready GMP education and implementation support for pharmaceuticals, biologics, medical devices, and specialty manufacturing—built for real inspection readiness.

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Ready Inspection-focused content
Aligned FDA • EU GMP • ICH
Practical Templates • Examples • Workflows
Compliance at-a-glance
Key frameworks we support
Learn GMP
FDA
21 CFR 210/211 • 820
EU GMP
Annex 11 • Data Integrity
ICH
Q7 • Q9 • Q10
Validation
CSV • IQ/OQ/PQ • VMP
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Built for GMP professionals

Training, consulting, and systems that support compliant execution—not just theory.

Pharma • Biotech • Medical Devices • Specialty Manufacturing

Training

Courses

Structured GMP learning with practical examples, quizzes, and real-world inspection scenarios. Free, premium, and hybrid course formats.

  • CSV / Data Integrity / Annex 11
  • Deviation • OOS • CAPA workflows
  • Validation & qualification fundamentals
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Consultancy

Services

Implementation support for inspection readiness, validation strategy, QMS setup, and data integrity. Delivered with documentation you can use.

  • Gap assessments & remediation plans
  • Inspection readiness (FDA/EU)
  • QMS design & rollout support
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Software

Digital QMS

Digital quality solutions designed to standardize execution, improve traceability, and support compliance. Built for regulated documentation and audit trails.

  • Deviations • CAPA • Change Control
  • Training management & records
  • Document control & tracking
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Regulatory-aligned, inspection-ready

Our approach emphasizes practical application, documentation discipline, and data integrity principles that support consistent GMP outcomes.

FDA
21 CFR Parts 210/211 • 820
EU GMP
Annex 11 • Data Integrity
ICH
Q7 • Q9 • Q10
Validation
CSV • IQ/OQ/PQ • URS/FS/DS

Why organizations choose Learn GMP

A clear, compliant path from training to execution.

Authority
10+
Years focus
100+
GMP topics
Ready
Inspection mindset
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Featured courses

Start with the most requested GMP topics.

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Computer System Validation

CSV • IQ/OQ/PQ • 21 CFR Part 11
Premium

Build a compliant CSV lifecycle approach with practical deliverables and audit-ready documentation.

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Out of Specification

OOS investigations • Root cause • CAPA
Hybrid

Learn a structured OOS process with decision trees, investigation discipline, and CAPA linkage.

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GMP Fundamentals

Core GMP principles • Documentation • QMS
Free

A practical foundation in GMP expectations, documentation discipline, and inspection behavior.

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Industries we support

Learn GMP supports teams working under strict quality and regulatory expectations across multiple manufacturing domains.

Pharmaceuticals
Biologics
Medical Devices
Radiopharmaceuticals
APIs & Oncology
Specialty Manufacturing

What you get

A disciplined approach that supports compliant execution.

  • Clear learning paths and practical examples
  • Templates, checklists, and real deliverables
  • Inspection readiness mindset and documentation standards
  • Support across training, consulting, and digital workflows
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Ready to strengthen GMP compliance?

Explore courses, request consulting support, or evaluate digital quality solutions for your QMS.

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