[dtwpb_yoast_breadcrumb]In-House Training Training and education for the pharma & biotech industry, since 1990.In-House GMP & GDP TrainingPCS has 33 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 Good Manufacturing Practices (GMP Basics & Expert) Good Distribution Practices (GDP Basics & Expert) Data Integrity Human Error Reduction Auditing & Self Inspections Risk Management Train the Trainer In-House Training OfferBelow 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. Internal & External Auditing Request Info Advanced Auditing Techniques Request Info FDA Inspection Preparedness Request Info Auditing QC Laboratories Request Info Auditing Aseptic Laboratories Request Info Auditing API / Excipient Suppliers Request Info Auditing Computerised Systems Request Info EngineeringProduction ProcessThe production process is the most important element within every pharmaceutical company. To retain control of this process is essential to adhering to GMP & GDP regulations. These PCS courses are designed to assist your company in controlling, upgrading and assessing your production processes.GxP Auditing TrainingAuditing (Inspection) of suppliers is a GMP & GDP requirement. PCS has a number of auditing courses which can be provided in-house. PCS can focus on your specific GMP & GDP Auditing procedures and/or policies.As we are working in a high-risk industry it is essential for engineering activities to be executed according to GMP & GDP regulations. PCS can help your Maintenance and Engineering departments develop a better understanding of these regulations and adapt accordingly. GEP (Good Engineering Practices) Request Info Equipment Management Request Info Water Systems Request Info Self-Inspection Techniques Request Info Equipment Maintenance Request Info Equipment Calibration Request Info Equipment Validation Request Info Validation Master Plan Request Info Sterilisation Process Request Info Sterilisation and Validation – Advanced Request Info Bio-Indicators Request Info Implementation of ASTM2500 (Risk-Based Qualification) Request Info Equipment Control during the Life Cycle Request Info Packaging Request Info Aseptic Production Request Info Environmental Monitoring Request Info Disinfection and Sterilisation Request Info Process Validation Request Info Risk Analysis of Production Processes Request Info Hygiene for Production Personnel Request Info Microbiology for Non-Microbiologists Request Info Cleaning Validation Request Info HACCP Request Info FMEA Request Info Principles of Contamination Control Request Info Critical to Quality Parameters (CQP) Request Info Critical to Quality Attributes (CQA) Request Info Quality Management SystemsQuality Management systems are difficult to implement, maintain or upgrade. PCS has a number of courses aimed at specific parts of a QMS which can be adapted to focus on your own Quality System. Documentation / System Management Request Info Setting up a CAPA System Request Info Deviation / CAPA Management Request Info Change Control Request Info Risk Management Request Info Third Party Contracting Request Info Contract Production Request Info Contract Analysis Request Info Training Systems Request Info Train the Trainer Request Info Supplier Qualification Request Info PQR (Product Quality Review Request Info Quality Control (QC)The Quality Control department is responsible for testing a variety of parameters. Whether its a complex finished product or a bag of talc, you want the tests to be accurate and according to GMP & GDP regulations. PCS can help your QC department reduce deviations and apply to regulatory requirements through its courses specifically designed for the Quality Control laboratory. GcLP (Good Control Laboratory Practices) Request Info Laboratory Equipment Management Request Info OOS (Out of Specification) Request Info Reagents and Standards Request Info Validation of Analytical Methods Request Info Validation of Microbiological Methods Request Info Stability Testing Request Info Transfer of Analytical Methods Request Info Handling RAW Data Request Info Implementation of LIMS Request Info Spread Sheet Validation Request Info General GxP CoursesThe following courses do not apply to a specific category but are designed to offer participants different levels of GMP & GDP related training. Process operators might benefit from a GMP Basic Course while upper management may benefit from a Quality Culture training or GMP Update seminar. GMP – the Basics Request Info GMP for Process Operators Request Info GMP for Mid-Level Management Request Info GMP for Upper Management Request Info GMP Awareness Request Info Quality Culture Request Info Annual GMP Update 2023 Request Info Good Distribution Practices (GMP) Request Info GMP for Biotechnological Products Request Info GMP – For the Entire Organization Request Info