Whether you’re bringing your first device to market, or you have launched multiple already, our upcoming True Quality Summit Series is for you. There’s a variety of different topics designed to provide best practices for advancing throughout your product lifecycle and maintaining compliance across multiple markets.
The Risk Management True Quality Summit Series will help quality, regulatory and product development professionals and executives understand and implement risk management concepts that can help meet FDA, ISO 14971, ISO 13485:2016, and the MDR 2017/745 requirements for risk management.
We’ll dive into the standards and outline deliverables at each stage of the risk management process, explore practical solutions for applying the standards within your organization, and ultimately give you tools to ensure risk management lives throughout your entire product life cycle.
Whether you've fully transitioned, are just getting started, or are planning to enter the EU market in the future, you won't want to miss this free virtual summit that covers common questions, pitfalls and strategies for operationalizing the requirements, and how to apply best practices to ensure ongoing compliance.
The two day, digital event dives into perspectives, predictions, and experiences of industry leaders and takes a deep dive into the insightful findings from Greenlight Guru’s State of Medical Device Product Development and Quality Management Report.
Now's your chance to uncover what it takes for your company to move forward and succeed in 2021.
The Greenlight Guru True Quality Virtual Summit is the must-attend experience for medical device quality, regulatory, and product development professionals who drive innovation in the most well-respected, high-performing companies in the market today.
