This document outlines the objectives and content of a training course on current good manufacturing practices (cGMP) and good manufacturing practices (GMP) in the pharmaceutical industry. The course aims to provide participants with basic knowledge of cGMP and GMP requirements. It covers topics such as quality management, sanitation, qualification and validation, complaints and recalls, contract manufacturing, self-inspection, personnel requirements, facility requirements, equipment, documentation, and good production and quality control practices. The target audience includes production and quality managers, pharmacists, chemists, and other roles involved in pharmaceutical manufacturing and quality.
This document outlines the objectives and content of a training course on current good manufacturing practices (cGMP) and good manufacturing practices (GMP) in the pharmaceutical industry. The course aims to provide participants with basic knowledge of cGMP and GMP requirements. It covers topics such as quality management, sanitation, qualification and validation, complaints and recalls, contract manufacturing, self-inspection, personnel requirements, facility requirements, equipment, documentation, and good production and quality control practices. The target audience includes production and quality managers, pharmacists, chemists, and other roles involved in pharmaceutical manufacturing and quality.
This document outlines the objectives and content of a training course on current good manufacturing practices (cGMP) and good manufacturing practices (GMP) in the pharmaceutical industry. The course aims to provide participants with basic knowledge of cGMP and GMP requirements. It covers topics such as quality management, sanitation, qualification and validation, complaints and recalls, contract manufacturing, self-inspection, personnel requirements, facility requirements, equipment, documentation, and good production and quality control practices. The target audience includes production and quality managers, pharmacists, chemists, and other roles involved in pharmaceutical manufacturing and quality.
Pharmacists, Chemists, Microbiologists, Supervisors, Officers, Technicians, Technician Assistants, QC Analysts, IPCU Inspectors, QA Inspectors, Transit Storekeepers, Storekeepers, Dispensing Area Staff, Preparation Area Staff, Archiving Area Staff, Packers, and anyone Interested In This Subject. Current & Good Manufacturing Practice for Pharmaceutical Industry Course Objectives • The participants will have the basic knowledge of what is GMP. They will know what is Quality Management and the requirements for a quality assurance unit • The participants will be able to review measures to ensure good sanitation in premises, personnel, equipment, apparatus and more.. • The participants will understand the basic aspects of qualification and validation & its scope • The participants will conceptualize complaint handling procedures and product recall procedures Current & Good Manufacturing Practice for Pharmaceutical Industry Course Objectives • The participants will have the basic knowledge on the general issues that arise when considering contract manufacture or analysis • The participants will identify the role of self-inspection in the quality management system • The participants will realize the general issues related to requirements & training for key personnel • The participants will know the key requirements for site choice and the specific requirements for main areas Current & Good Manufacturing Practice for Pharmaceutical Industry Course Objectives • The participants will be able to discuss problems related to issues around selected items of equipment. • The participants will be familiarized with specific requirements for each type of material(from starting to waste material) • The participants will gain the basic documentation skills needed in order to fulfill all pharmaceutical requirements • The participants will be able to discuss aspects of good practices in production and quality control Current & Good Manufacturing Practice for Pharmaceutical Industry Course Index • Introduction to the • Self Inspection and training program quality audits • Quality Management • Personnel • Sanitation and hygiene • Premises • Qualification and • Equipment Validation • Documentation • Complaints and recalls • Good Practices in • Contract production production and and analysis quality control Ask for arrangement of a training course for your company now please contact upbeat consult at Mobile +962 796362237 or land line +962 6 5515451 Amman- Jordan office or You Can Send us an E mail to info@upbeatconsult.com www.upbeatconsult.com Skype: upbeatconsult