Medıcal devıce

We utilize years of hands-on experience to ensure our clients to get their products to market as efficiently as possible. We can compile, submit, and manage all your device registrations and all post-registration, follow-up processes via “Product Tracking System (UTS)” Our experienced consultants can review your Technical File, register your medical device or IVD, as required and respond to any questions or concerns from the Competent Authorities.

We provide post-market compliance solutions, incident reporting, and global vigilance support informed by a life-cycle approach to device safety and effectiveness.