Gain confidence that your product meets the necessary quality standards and ensure compliance with the guidance of seasoned experts. Susan Schniepp, who brings 40 years of high-level quality assurance experience in the pharmaceutical industry, will lead a 90-minute panel discussion alongside Seyed Khorashahi and Steve Lynn from Regulatory Compliance Associates® Inc.
This panel discussion aims to provide valuable insights and practical advice to help you prepare, organize, and streamline your audit approach. The session will focus on identifying quality issues and working with clients to establish more robust operations that can withstand regulatory scrutiny. Attendees will benefit from the combined expertise of the panelists, who will share their experiences and strategies for achieving compliance and enhancing quality assurance processes.
Key topics to be covered include best practices for audit preparation, effective organization of audit activities, and methods for streamlining audit processes to identify and address quality issues promptly. The panel will also discuss solutions for collaborating with clients to develop comprehensive strategies that ensure regulatory compliance and improve operational robustness.
By participating in this discussion, professionals in the pharmaceutical and medical device industries will gain actionable insights to enhance their quality assurance practices. This knowledge is crucial for maintaining compliance with regulatory standards and ensuring the highest levels of product quality.
This panel discussion is essential for quality assurance, regulatory affairs, and compliance professionals looking to strengthen their audit approaches and ensure their operations can withstand rigorous regulatory scrutiny. Join us to learn from industry veterans and take your quality assurance and compliance efforts to the next level.