Creating a Regulatory Roadmap for MedTech Market Success with Etienne Nichols

In this episode of the Global Medical Device Podcast, Etienne Nichols sits down with Adnan Ashfaq of Simplimedica, a seasoned quality, regulatory, and validation specialist, to explore the critical role of developing a regulatory roadmap for medical device companies.

Adnan breaks down the differences between a regulatory strategy and a regulatory roadmap, highlighting how a well-designed roadmap serves as a guiding document for market access and investor confidence. The conversation delves into navigating complex market regulations, assessing classification and compliance needs, and identifying strategic global market entry opportunities.

Adnan’s 25+ years of experience provide actionable insights for medtech startups and established companies.

The original article can be found here.

Simplimedica offers a Regulatory Roadmap writing service. For further details, click here.