Simplifying Regulatory Pathways

We at EZ Reg are motivated to make the regulatory pathways for startups in the healthcare and medical device space simple, lean and fast.

About Us
Saving money in the long run

On an average $24M to $75M USD spent on regulatory activities by medical device companies, let's plan in advance to ensure success.

Understanding regulatory needs at research phase

From an initial stage it's important to be aware of regulatory challenges, non-compliance costs medical device startups millions of dollars per year. Let's help you prevent that.

Helping understand FDA requirements

510(k)s, PMAs, QSR needs...
We help you understand all regulatory jargons!


Madhuri Iyer

Mechanical Engineer, Mathematician and an RAQA enthusiast passionate about developing innovative medical technologies.

Amanda C├ęspedes

Serial Entrepreneur, Biotechnology Engineer, Regulatory Affairs Professional with RAPS certifications in medical devices and drugs.

Get in Touch

In case of any questions please...
Contact us!

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