The aim of this course is to provide a comprehensive understanding of applying the concept of quality assurance on the whole process. The course places strong emphasis on main objectives of quality assurance like regulatory requirements, quality management systems, and quality control steps involved to maintain compliance with the current Good Manufacturing Practices (cGMP) standards.

Through this course, participants will become familiar with the global standards, rules and regulations for quality assurance. It seeks to clarify the concepts of quality management systems and their applications, methods of quality control, validation and verification techniques, ethical laboratory practices along with proper documentation. It also gives an understanding about conducting audits, inspections and thereby carrying out corrective and preventive actions. This will enable a professional to maintain the quality and contribute to the overall safety factors in pharmaceutical production.