Navigating the Evolving Regulatory Landscapes
15/4/2025
Join us for an insightful fireside chat, where industry experts from Global Regulatory Services (GRS), Med-Di-Dia, and BioPortUSA will discuss the current and upcoming regulatory landscapes in the US and EU.
Register NOW!! 01 May 2025 2:30 - 4:00 PM UK/Irish time
This webinar is tailored for startups, SMEs, and companies planning to enter or expand in these markets. Our speakers will discuss the latest regulatory changes, including a case study on the Google Pixel Watch's recent EU-first, US-second regulatory approach, and provide strategic insights into navigating these complex environments.
Speakers:
Key Discussions:
- Overview of US and EU Regulatory Frameworks
- Strategic Compliance Pathways
- Approaches to choosing the right compliance pathway for successful market entry.
- The role of regulatory strategies in product success.
- Adapting to Regulatory Changes
- Anticipated US and EU regulations updates and how to prepare for them.
- The shift from QSR to QMSR and its business implications.
- Regulatory Strategy Analysis: EU First or US First
- A comparative look at the benefits and challenges of launching products in the EU versus the US. [Taking Google Pixel Watch 3 as a case study]
- Interactive Q&A
Who Should Attend:
- Entrepreneurs and startups in the MedTech sector.
- SMEs looking to expand their footprint in the US and EU markets.
- Regulatory and compliance professionals in the healthcare industry.
Register Now to secure your spot and gain valuable insights into the complex world of MedTech regulations. Whether you're looking to launch a new product or navigate regulatory submissions, this webinar will equip you with the knowledge and strategies needed for success.
