In less than 10 minutes you will learn how to enter your medical device in the U.S. Market. This short video provides an overview of the steps required to get your medical device cleared by the US FDA. From establishment registration and device listing to preparing your 510(k) submission, this brief tutorial provides pertinent information.
MAVEN PROFCON SERVICES LLP is an India based regulatory consultancy for various certifications of Medical Devices and Personal Protective Equipment.
We strive to foster innovative services that will contribute substantially to our customer’s success. We provide consultative technical and regulatory expertise. Our team is empowered to build trust at every step.
We work closely with our clients to ensure all communications and regulatory requirements are transparent and clearly addressed in a timely manner.
Our innovative passionate and result-driven professionals to make MAVEN what it is today; providing innovative approaches and exceptional service to customers all over the world.
Our highly performant team members possess vast expertise in regulatory consulting, medical device engineering, quality assurance, digital and business intelligence and many with medical device industry experience in technical fields.
We deliver robust, scalable solutions with increased quality and 100% Output.
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