For Pharma & Biotech
PCS has 33 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.
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.
GMP – the Basics
Request InfoGMP for Process Operators
Request InfoGMP for Mid-Level Management
Request InfoGMP for Upper Management
Request InfoGMP Awareness
Request InfoQuality Culture
Request InfoAnnual GMP Update 2023
Request InfoGood Distribution Practices (GMP)
Request InfoGMP for Biotechnological Products
Request InfoGMP – For the Entire Organization
Request InfoDocumentation / System Management
Request InfoSetting up a CAPA System
Request InfoFMEA
Request InfoDeviation / CAPA Management
Request InfoChange Control
Request InfoRisk Management
Request InfoThird Party Contracting
Request InfoContract Production
Request InfoContract Analysis
Request InfoTraining Systems
Request InfoTrain the Trainer
Request InfoSupplier Qualification
Request InfoPQR (Product Quality Review)
Request InfoPackaging
Request InfoAseptic Production
Request InfoEnvironmental Monitoring
Request InfoDisinfection and Sterilisation
Request InfoProcess Validation
Request InfoRisk Analysis of Production Processes
Request InfoHygiene for Production Personnel
Request InfoMicrobiology for Non-Microbiologists
Request InfoCleaning Validation
Request InfoPrinciples of Contamination Control
Request InfoCritical to Quality Parameters (CQP)
Request InfoCritical to Quality Attributes (CQA)
Request InfoInternal & External Auditing
Request InfoAdvanced Auditing Techniques
Request InfoFDA Inspection Preparedness
Request InfoAuditing QC Laboratories
Request InfoAuditing Aseptic Laboratories
Request InfoAuditing API / Excipient Suppliers
Request InfoAuditing Computerised Systems
Request InfoEquipment Management
Request InfoWater Systems
Request InfoSelf-Inspection Techniques
Request InfoEquipment Maintenance
Request InfoEquipment Calibration
Request InfoEquipment Validation
Request InfoValidation Master Plan
Request InfoSterilisation Process
Request InfoSterilisation and Validation – Advanced
Request InfoBio-Indicators
Request InfoImplementation of ASTM2500 (Risk-Based Qualification)
Request InfoEquipment Control during the Life Cycle
Request InfoDownload our training brochure for 2024 by clicking this link