Expert Regulatory and Quality Consulting

FDA, EU, Health Canada and More

Our Services

At EZ-RA, our consulting services provide comprehensive support throughout the lifecycle of your Medical Devices, Pharmaceuticals, NHPs, Foods, and Cosmetics, from initiation to post-market phases

FDA 510(k), PMA , 513(g), Pre-Submission etc.

FDA Cybersecurity Documentation & Testing

Internal/External Audit Support

Health Canada & EU MDR

Clinical Strategy/Planning

Market Access – Middle East, Africa, South America, APAC

About Us

Your Trusted Partner in Regulatory and Quality Excellence.

Compliance Made Easy

Expertise & Guidance

Backed by more than two decades of industry expertise, we deliver high-impact regulatory and quality consulting tailored to your product’s path. Our services blend rigorous technical knowledge with strategic foresight to ensure smooth progression from development to commercialization. We help teams achieve compliance with confidence.

Market Readiness

Whether you’re a startup or multinational, we are committed to ensuring your product’s success in the global market while navigating the ever-evolving regulatory landscape.