Tailored for your team
In-House Training
Design GMP and GDP training around your processes, people, and quality challenges with PCS Academy.
For Pharma & Biotech
In-House GMP & GDP Training
For 35 years, PCS has run GMP and GDP training inside manufacturers, wholesalers, hospital pharmacies, contract laboratories and the suppliers around them. In-house means the syllabus, workshops and worked examples are rebuilt around your products, your SOPs and the findings you actually need to close — not a generic deck.
Most Popular In-House Training
- GMP Refresher
- GMP Awareness
- Data Integrity
- Human Error Reduction
- GMP for Mid-Level Management
In-House Training Offer
A selection of in-house courses below. The catalogue is not exhaustive. If what you need is not listed, get in touch and we will build it.
General GxP Courses
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GMP – the Basics
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GMP for Process Operators
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GMP for Mid-Level Management
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GMP for Upper Management
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GMP /GDP Awareness for Senior Management
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GMP Awareness for Operational Staff
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GMP Awareness
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Quality Culture
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Annual GMP Update 2026
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Good Distribution Practices (GMP)
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GMP for Biotechnological Products
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GMP for Radiopharmaceuticals
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GMP – For the Entire Organization
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Quality Management Systems
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Documentation / System Management
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Setting up a CAPA System
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FMEA
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Deviation / CAPA Management
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Change Control
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Risk Management
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Third Party Contracting
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Contract Production
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Contract Analysis
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Training Systems
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Train the Trainer
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Supplier Qualification
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PQR (Product Quality Review)
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Production
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Packaging
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Aseptic Production & Contamination Control
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Environmental Monitoring
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Disinfection and Sterilisation
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Process Validation
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Risk Analysis of Production Processes
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Hygiene for Production Personnel
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Microbiology for Non-Microbiologists
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Cleaning Validation
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Principles of Contamination Control
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Critical to Quality Parameters (CQP)
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Critical to Quality Attributes (CQA)
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GxP Auditing Training
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Global Auditor Certification Program
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Internal & External Auditing
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Advanced Auditing Techniques
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FDA Inspection Preparedness
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Auditing QC Laboratories
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Auditing Aseptic Laboratories
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Auditing API / Excipient Suppliers
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Auditing Computerised Systems
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GxP Engineering Training
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Equipment Management
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Water Systems
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Self-Inspection Techniques
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Equipment Maintenance
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Equipment Calibration
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Equipment Validation
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Validation Master Plan
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Sterilisation Process
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Sterilisation and Validation – Advanced
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Bio-Indicators
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Implementation of ASTM2500 (Risk-Based Qualification)
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Equipment Control during the Life Cycle
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