GRS News

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:

• Jacob Skinner, Med-Di-Dia
• Michelle Bonn, BioportUSA
• Greer Deal, GRS
• Mark Lesselroth, BioPortUSA

 

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.

 

Click here to Register