Unlocking Success: Quality, Compliance, and Commercialization in MedTech
Join us for the Regulatory Affairs Professionals Society (RAPS) & API event, where we’ll explore quality management, regulatory compliance, and commercialization strategies for startups in Medical Devices, Diagnostics, and Digital Health. Don’t miss the presentation, “Quality and Compliance – Why Are They So Important to My Startup?” Discover actionable strategies to overcome regulatory hurdles, leverage quality as a competitive edge, and navigate the latest compliance challenges. Get equipped with key market entry and quality management insights and practical advice to uphold high regulatory standards.
Following the expert presentation is a dynamic panel discussion, “From Concepts to Market: Overcoming Early Challenges and Strategies for Successful Medical Device Commercialization” Hear from top industry leaders, experts, and innovators who will share their experiences and strategies on tackling sector-specific challenges, achieving quality-driven success, and what investors seek in thriving startups.
Cap off the event with valuable networking opportunities, gaining direct advice on building a robust foundation for growth and innovation in the fast-paced world of Medical Devices, Diagnostics, and Digital Health.
Seize this chance to arm your startup with the knowledge and tools needed to excel in the competitive life sciences arena!
Event note; in-person capacity is at 100 individuals. Guests who register after the cap has been made can participate via a hybrid model. A link will be sent to those guests prior to the event.
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Sector: Medical Devices, Diagnostics/IVDs, Digital Health/SaMD/AI
Professional Interest: Compliance, Quality Assurance and Control; Product Development