We were created to create CADCAM PSI
CADskills designs and manufactures state of the art custom made solutions for your patient. We trust in our existing innovative concepts that are created and perfected by experts in their field. The state of the art implants are biofunctionalized.
Also, our CADskills team offers support to the development of an idea and implementation of an R&D strategy. We help you taking care of your intellectual property by writing and filing patents and we help with finding funding for research.
After communicating with the surgeon, we design, structurally analyze, manufacture and biofunctionalize the implant for an optimal clinical result.
Today, CADskills manages nearly all tasks in-house with a dynamic and enthusiastic team.
In 2018 the portfolio expanded with patient-specific concepts for orthopaedic surgery, in cooperation with influential surgeons in the field of hand, shoulder and elbow surgery. CADskills is always looking for new opportunities, so do not hesitate to contact us.
Also, basic and translational research and development make up a great part of our activities. In this way CADskills is always revolutionizing, inspired by both surgeons and engineers.
CADskills is expanding its distribution network inside Europe.
We are looking for companies who are as passionate as we are about using state-of-the-art technology to help surgeons and patients.
Do you have already an existing network of CMF / MaxFac/ OMF / Neuro surgeons? Feel free to contact our team of specialists.
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Medical consultancy
Prof. L. De Wilde (shoulder)
Dr J. Duerinckx (hand & wrist)
Prof. M.Y. Mommaerts (CMF)
Prof. Em. I. Naert (prostho)
Dr. G. Van den Bogaert (knee)
Dr. F. Verstreken (hand & wrist)
Dr. Ph. Winnock de Grave (knee)
Dr. K. Buedts (foot)
Dr. Casper Van den Borre (CMF)
CADskills is actively pursuing essential certifications, specifically ISO 13485:2016 and MDR 2017,/745 to enhance its position in the medical device industry. ISO 13485 focuses on quality management systems for medical devices, ensuring that products are developed and manufactured to the highest standards of quality and safety. The MDR, or Medical Device Regulation, represents a commitment to the safety and effectiveness of medical products, ensuring that consumers receive reliable and compliant solutions.
By partnering with Covartim, a consultancy with expertise in regulatory compliance, CADskills is navigating this journey effectively. Additionally, collaborating with the BSI Group, a recognized notified body, will provide the necessary support and audits to ensure adherence to these important standards. Through these efforts, CADskills is not only improving its offerings but also enhancing its credibility and trust in the market.We are compliant with the latest amendments (Regulation (EU) 2023/607) to the MDR transition period, and registered with the Belgium Competent Authority (FAMHP).
With the support of our authorized representative, Qarad, our products are also commercialized in the UK and Switzerland.