MEDIcept strives to provide our clients with proven, trusted, and cost-effective solutions. We are an international consulting firm specializing in medical device, IVD, and biotechnology Regulatory, Quality, and Clinical Services. Since 1996, we have worked with thousands of companies to solve their most critical FDA and ISO issues. Our integrated solutions are rooted in our direct experience and span all stages of the product life.

Our staff includes former FDA and Notified Body personnel and industry experts with an in-depth functional knowledge of medical devices. Medical device compliance requires the navigation of a complex maze of requirements. MEDIcept can provide state-of-the-art interpretation of regulations, guidance documents, and standards and provide clients with the information they need to comply safely and cost-effectively.

We use our expertise to quickly identify the root cause, coalesce corrective actions, and provide easy to understand structured solutions. Since we know corrective action implementation is where many projects fail, we don’t just write an action list. We make sure all stakeholders understand why the solutions were chosen and why they are needed. We work hand-in-hand with clients to implement the solutions, so the solutions have been culturally absorbed when the project is done.

MEDIcept is committed to providing our clients with what they need. We are committed to quality deliverables because we value our clients’ time and resources. This is why 90% of our clients come back to us repeatedly to solve new issues and recommend us to their colleagues.