How quality management drives continuous improvement for life sciences organizations
Discover an insightful webinar that explores how quality management can serve as a catalyst for continuous improvement for life sciences organizations to evolve in an ever-changing regulatory landscape.
With evolving regulatory landscapes and increasing industry demands, staying ahead requires more than compliance – it requires the ability to innovate and improve consistently. During this webinar, the expert speakers will shed light on the shifting regulatory expectations surrounding quality and examine the latest trends shaping the life sciences sector. They will also demonstrate how modern quality management systems (QMS) can go beyond compliance and act as a foundation for identifying opportunities and implementing impactful improvement initiatives.
This is an excellent opportunity for attendees to gain a deeper understanding of how QMS tools can be utilized in real-world scenarios to optimize processes, enhance efficiency and meet both operational and compliance goals.
Watch on-demand today to understand the importance of proactive quality management in challenging and fast-evolving industries.
Joanne Rupprecht is a seasoned expert in quality and regulatory affairs, federal agency/life sciences law and higher education with over 35 years of experience in healthcare product development across academia and industry. She specializes in domestic (FDA) and international regulatory systems for medical devices, pharmaceuticals, biologics, CAR T cell and stem cell therapies and vaccines.
Jo’s career began with research and development roles at the University of Illinois, the University of Chicago and Abbott Laboratories. She has contributed to key industry resources, including RAPS’ regulatory affairs manuals and taught biomedical entrepreneurship and regulatory environment courses at the University of Colorado, Denver. Jo also served on the BESST Program Board at the Anschutz Medical Campus.
She earned her Juris Doctor from the University of Denver Sturm College of Law and later received a Life Sciences Compliance Certification from Seton Hall University. Jo holds multiple professional credentials, including RAC (US and Global), ACRP-CP, CCEP and ACUE, and is a Fellow of the Regulatory Affairs Professionals Society (FRAPS).
Anthony Gruttadauria is a trusted expert in healthcare and life sciences, specializing in enhancing compliance and streamlining quality processes. With extensive knowledge of ISO standards, GxP requirements, ICH guidelines and FDA regulations, he helps organizations thrive in complex, regulated environments.
Anthony’s collaborative approach sets him apart. Working closely with quality leaders, he develops practical solutions tailored to organizational needs and builds efficient, audit-ready operations that stand up to regulatory demands. His passion extends beyond compliance, focusing on empowering teams with the tools and strategies needed to improve product integrity and foster continuous improvement across quality programs.
Dedicated and insightful, Anthony transforms complex regulations into actionable strategies, supporting organizations in achieving their goals while driving sustainable success.
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