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In-House Training
For Pharma & Biotech
In-House GMP & GDP Training
PCS has 34 years of experience in providing training to GMP and GDP regulated organizations. This includes manufacturers, distributors, laboratories, hospitals, pharmacies and related industries. An advantage of our in-house training courses is that the program, training content, workshops, exercises and methodology can be adapted to suit the specific needs of your company.
Most Popular In-House Training
- GMP Refresher
- GMP Awareness / GDP Awareness
- Data Integrity
- Human Error Reduction
- GMP for Mid-Level Management
In-House Training Offer
Below you will find an overview of some of our internal training courses. The list below is not all-encompassing. Contact PCS if the training you are looking for is not listed.
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 Awareness
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Quality Culture
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Annual GMP Update 2023
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Good Distribution Practices (GMP)
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GMP for Biotechnological Products
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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
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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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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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