The Medical Device Innovation Consortium Annual Public Forum will bring together MDIC members and the broader medical device and diagnostics community to discuss current trends in regulatory science and reimbursement as well as highlight the development of innovative regulatory science tools. The attendees will also get the opportunity to hear from industry experts, patients and other community innovators on a range of regulatory topics from cybersecurity and real-world evidence to patient input, quality, and innovative medical device developments.
Don't miss the twelfth annual Washington State Medical Device Summit scheduled for Thursday, September 19. Hosted by the Biomedical Device Innovation Partnership Zone located in Bothell, Washington, the Summit program brings together leading executives, entrepreneurs, researchers, government officials, thought leaders, and stakeholders from the medical device community to explore the state of the industry and the trends and innovations coming our way; review the current opportunities and challenges for the region; and learn more about the resources available within Washington State's life science ecosystem.
CLARIFYING PATIENT-CENTERED POLICY: A FRAMEWORK FOR INCORPORATING PATIENT PERSPECTIVES IN FDA REGULATORY DECISION-MAKING
Join me at the RAPS Convergence 2019 in Philadelphia for my session focused on patient-centered regulatory policy. More details to come on the panel speakers. Don’t miss the best regulatory conference in the U.S. See you in Philadelphia!
INCLUDING PATIENT EXPERIENCE DATA IN REGULATORY DECISION MAKING
I am honored to be invited to speak at the Saudi Food and Drug Administration (SFDA) Annual Conference. I am excited to share the different ways that patient experience data can be included in regulatory decision-making.
The European Patients’ Forum has been representing patients’ voices in a united and influential way over the past 15 years to drive better health in Europe. This event will provide an exceptional opportunity for dialogue, engagement with a wide range of health players who aspire to make patient involvement a reality. Together, we will explore why this will lead to better outcomes for patients and society, and how we can achieve this in practice across the European Union.
The 2019 Regulatory Alliance Forum, hosted by AcKnowledge Regulatory Strategies, will take place on August 19-21, 2019 in San Diego, California.
The conference will primarily focus on FDA regulatory topics and updates to US medical device regulations. All of our speakers are former-FDA employees who worked at the Center for Devices and Radiological Health.
FDA’S PATIENT PREFERENCE INITIATIVE - WHAT DOES IT MEAN FOR THE MEDICAL DEVICE INDUSTRY?
Join me at the 9th Annual 10x Medical Device Conference where I will be speaking about FDA’s Patient Preference Initiative (PPI) and it’s relevance to the medical device industry. I hope to see you there!