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This comprehensive resource covers product change evaluation, postmarket surveillance, audit/inspection compliance, and various other laws and regulations pertaining to maintaining a product on the market.
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
This is an on-demand recording from June 22, 2022
Quality, compliance and regulatory professionals love standardization - and your auditors will look for it too. Doing the same things the same way across your business slices risk, strengthens your processes and embeds robust, repeatable quality.
Targeted audits and inspections are your secret weapon for driving a standardization program that actually works. Join our webinar to hear top tips and tactics, mistakes to avoid and detailed guidance to start working to a stronger, more standardized business operation.
After this program, participants will:
Director Of Quality, Qualio
Kelly leads Qualio’s in-house quality team and spearheads the company's Qualio+ QA support service. Kelly has built over 20 years of experience working with quality teams at Abbott, Sandoz, Cochlear and more, before becoming Qualio's Director of Quality.
Regulatory Director, Rimsys
Bruce is Regulatory Director of Rimsys and has amassed over 25 years of quality and regulatory experience. With a focus on quality management and international regulatory compliance, Bruce has worked with electromechanical, implantable and SaMD organizations.
RAPS reserves the right to cancel this program at its sole discretion. RAPS will not be responsible for travel or other costs incurred due to cancellation.
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