The Benefits, Risks and Future of ePTFE
The use of ePTFE in medical devices has enormous advantages, but getting it right requires deep expertise. Join us as we explore the benefits, risks, and mitigation strategies, along with…
Richardson Waiver Repeal: What it Means for Medtech
Sidley Austin, joined by HPA, led a program examining the impact of HHS repealing the so-called “Richardson Waiver”, including its history, how it could impact the activities of the U.S.…
Tariffs: Navigating Customs Origins Requirements for tariffs, USMCA exemptions and beyond (Members Only)
Exclusive member webinar on tariffs, customs, USMCA rules of origin, and compliance strategies with expert Larry Friedman. Air Date April 4, 2025. Now On Demand!
Navigating Inbound Trade & Investment: Strategies for Medtech in the Era of Tariffs & Trade Legal and Policy Shifts
Akin will provide a CLE program covering the latest legal issues for inbound trade and investment, including the Trump Administration’s approach to trade policy and tariff issues, and strategies medical…
Tariffs 101: Understanding the Impact of New Tariff Policies (Members Only)
This educational primer will break down tariffs, trade policies, and legal frameworks—giving you the basics you need to navigate upcoming changes.
Game-Changing Compliance Education for Healthcare Professionals: Healthstream Webinar
AdvaMed® offers members compliance education and ethical guidance for interactions with healthcare professionals through the HealthStream-powered AdvaMed® Code of Ethics. Demo this important tool during this webinar.
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…
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.
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.