The course will cover: Warehouse Good Manufacturing Practice (GMP), Good DistributionPractice (GDP), Good Storage Practices (GSP) and Qualification Process,Temperature/Humidity MappingWarehouse Material SystemWarehouse DesignReferences: PIC/S, WHO, FDA, SAPHRA LEARNING OUTCOME Understanding of the Warehouse GMP, GDP, GSP requirementsUnderstanding the Qualification ProcessUnderstanding Temperature and Humidity Mapping ProcessUnderstanding of computer systems and their importance (Warehousemanagement systems)Understanding WHO, FDA, SAPHRA Guidelines

CST Val Consulting & Services (South Africa) in collaboration with PharMatrix (Bahrain and Jordan) proudly presents the First Pharmaceutical Industry Classroom Workshop & Training Week, titled Pharmaceutical Quality, Validation and Engineering Training Workshop This exclusive event will feature the following: 1st Workshop (Two Days) : Risk Based Approach in Cleaning Validation as per EMA and ISPE (19th -20th May 2025) […]

Quality Risk Management (QRM) principles require the systematic evaluationof risk, patient safety and product quality based on scientific knowledge, dataand experience.Regulatory bodies expect QRM to be seamlessly integrated into the QualityManagement System (QMS) framework by using the life cycle approach. Thisintegration involves the implementation of both formal and informal riskassessment tools that support the elements defined in ICH Q9 for […]

This 3 day course will cover important pharmaceutical utility systems that areimportant for proper functionality of the manufacturing plant, such as:Water (Potable Water, Purified Water and Water for InjectionSteam (Plant, Industrial)Pure Steam/Clean SteamSystem and Process Gases (Compressed air, Nitrogen). References: ISPE Baseline Guide – Water and steam systemsApproaches to commissioning and qualifications of pharmaceutical waterand steam systems.Sampling for pharmaceutical water, […]