2 Day Medical Device Design Control Course: Streamline Development and Guarantee Top-tier Quality and Compliance
DUBLIN, Nov. 17, 2023 /PRNewswire/ -- The "Medical Device Design Control Essentials Course" training has been added to ResearchAndMarkets.com's offering.
Participate in our immersive 2-day virtual seminar to acquire essential knowledge and establish robust processes for Design Controls in the production of safe and effective medical devices. Recognized as a critical process by the FDA, Design Controls are vital for ensuring compliance and quality in the medical device industry.
Despite their importance, Design Controls often lead to frequent 483 and Warning Letter observations. In this seminar, we will guide you on how to effectively integrate Design Controls into your product development process. This integration not only streamlines development but also guarantees top-tier quality and compliance.
Our seminar is tailored exclusively to Design Controls for medical devices, providing a deep understanding of the essential requirements and how to efficiently translate them into processes customized to your company's unique needs. Delve into the history, context, and specific requirements of design controls, and explore detailed tools and techniques.
Engage in practical exercises that will enhance your skills and refine your design control process. Don't miss this opportunity to stay ahead in the medical device industry by mastering the art of Design Controls.
WHY YOU SHOULD ATTEND:
To prevent such quality and compliance issues, implementing a rigorous and efficient design control process is crucial. Identifying and addressing issues early on leads to faster resolutions and safeguards against costly setbacks. Join our seminar to gain valuable insights and strategies to avert design problems and their detrimental impact on quality, cost, speed to market, and customer satisfaction.
Addressing and rectifying these issues early in the design phase yields far greater leverage compared to addressing problems in already-produced products. Our webinar offers an opportunity to learn from past issues, enabling you to enhance the quality and performance of your future product generations.
They will come away with key concepts, practice in these concepts, and extensive course notes for future use and reference:
Who Should Attend:
DAY 1 (10 AM to 3 PM)
DAY 2 (10 AM to 3 PM)
Susanne also holds Regulatory Affairs Certification (RAC) from RAPS and Certified Quality Auditor (CQA) certification from the American Society for Quality. Susanne has now established a consulting business with a mission to provide services to help medical device companies achieve world-class quality and compliance.
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