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Our Services

corporate service

We Are the Best Medical device Regulatory experts

We strive to foster innovative services that may contribute well to our customer’s success.

  • Industrial expertise and relevant education backgrounds
  • Customised solution for every client
  • Confidential and transparent communication
  • Support post-certification
  • Multiple allied services so all needs can be catered at once
  • Continuously evolving & and adapting to keep up with state-of-the-art practices
what we do

Our Services Makes Your Regulatory Submissions Effortless

Client confidentiality and satisfaction being our objective, we offer an array of services with respect to regulatory requirements globally and have allied with various other service providers for different aspects of certifications so that clients can have a single entity to deal with while we coordinate on their behalf.

CE Certification
US FDA 510(k)

We have collaborated with MAVEN on several clinical trials for medical devices. Their regulatory support has consistently ensured our studies adhere to all applicable guidelines. Their expertise and reliability have made them an invaluable partner in our mission to advance healthcare.

Emily Roberts

Maven played a pivotal role in our CE certification journey, guiding us through the maze of medical device regulations. Their expertise and dedication ensured our product met all requirements. Thanks to their support, we successfully launched our medical device on the market.

Sarah Johnson

As a startup founder, I was overwhelmed by the regulatory challenges in the medical device industry. Maven Profcon Services LLP became our guiding light, helping us at every turn. Their knowledge and professionalism were instrumental in gaining regulatory approval, making our dream a reality.

James Martinez