Duration: 90 Minutes
This comprehensive training session on the International Council for Harmonization (ICH) Q9 guideline, with a special focus on the revised version, ICH Q9(R1). Gain a deep understanding of the fundamental principles, concepts, and practical application of the risk management approach as outlined in this esteemed guideline. Discover how these principles directly impact the pharmaceutical industry and learn about the various applications and cutting-edge tools employed for effective Quality Risk Management. Benefit from real-world examples illustrating the application of these tools.
By participating in this training program centered around ICH Q9(R1), you will acquire the essential knowledge and skills needed to successfully implement quality risk management principles. Achieve regulatory compliance, enhance your quality systems, reduce costs, make informed decisions, foster cross-functional collaboration, and cultivate a culture of continuous improvement within the pharmaceutical sector.
Why You Should Attend:
Upon completion of this training, you will possess a solid foundation in ICH Q9(R1) and its guiding principles. Empowered with this expertise, you will be able to seamlessly integrate risk management practices into your respective roles within the pharmaceutical industry. Contribute to elevated product quality, heightened patient safety, and unwavering regulatory compliance, ultimately driving excellence in every facet of your organization.
Areas Covered in the Session :
Who Should Attend: