AdvaMed 2025 State Policy Briefing: Data Privacy
Hear from AdvaMed’s data privacy expert, Terry Chang, on the critical exemptions we seek in comprehensive data privacy laws across the country.
Digital Health
Learn more about our Digital Health work.
AdvaMed 2025 State Policy Briefing: AI in Healthcare
AdvaMed’s digital health policy expert, Geeta Pamidimukkala, and payment and health care delivery policy expert, Kirsten Tullia, break down how artificial intelligence and machine learning (AI/ML) technologies are transforming patient…
The Art of the MedTech Real Estate Deal – Accelerating Innovation & Mitigating Risk Webinar
Jones Lang Lasalle Inc. is the trusted real estate advisor to over 100 AdvaMed members across the globe and will be presenting the tools and strategies they have employed to…
AdvaMed Commends House AI Taskforce’s Recommendation to Ensure Reimbursement, Expand Access to AI-Enabled Medical Devices
AdvaMed, the Medtech Association, commended the House of Representatives’ bipartisan Task Force on Artificial Intelligence for urging the Centers for Medicare & Medicaid Services (CMS) to develop a formalized payment…
Strategic Risk Assessment in Medical Device Compliance: Proactive Strategies for Effective Risk Management Webinar
Join Porzio in this session that will help med device compliance leaders with messaging, designing, and implementing risk assessments, a key component of an effective healthcare compliance program.
Life Sciences Strategy and Innovation
This white paper explores the evolution of current biopharmaceutical commercial models. By addressing key considerations essential for every healthcare leader, this shares the impact of integrating digital assets clinician engagement…
Transforming Digital Innovation to Business Reality in Life Sciences
The industry is at the forefront of physical and digital technologies, with implications for research, development, manufacturing and patient care. Digital technologies and workflows can unlock discoveries, leading to new…
Being a Trusted Advisor to Medical Device C-Suites During Government Investigations Webinar
Join King & Spalding for this engaging panel that will cover common experiences and practical considerations for advising medical device company executives during a government investigation.
Preparing for the FDA’s Quality Management System Regulation (QMSR) Rollout in 2026 – Understanding the changes and aligning with ISO 13485 Webinar
Join Lachman Consultants for a webinar that will equip medical device companies with the knowledge to navigate the upcoming FDA QMSR changes set for 2026.
The AI-Enabled Supply Chain: End-to-End Visibility and Enhanced Decision-Making Webinar
Join EPAM for an engaging webinar that explores how AI is reshaping the supply chain into a data-rich environment.