Simon Baker

During this session, we'll delve into the responsibilities of the Qualified Person (QP) within clinical packaging organizations, with a particular emphasis on assessing implications for patient safety and predicting forthcoming regulatory changes.

Key Takeaways:

• Gain insights into the multifaceted role of the Qualified Person in ensuring compliance, quality, and patient safety
• Stay updated on the latest regulatory developments impacting QP responsibilities, including labeling requirements, temperature control standards, and serialization mandates.
• Prepare for the future regulatory landscape by anticipating emerging trends, technological advancements, and potential changes in global regulatory frameworks affecting QP practices.