The medical device industry is as competitive as any. And the process of concepting, designing, testing, manufacturing and marketing a device can be fraught with considerable challenge and risk. This is where Invibio pledges to go the extra mile. Not only can you depend upon the performance of our exceptional biomaterials, but also on our genuine commitment to provide insight and consulting throughout the entire process to help you realize your goals faster.

• Incubation: OEMs often approach us when their ideas are still on the drawing board, which is something we encourage. At this early stage, we can usually provide insights and suggestions that help improve a product's overall efficacy as well as create efficiencies through the regulatory, manufacturing and marketing phases.
• Regulatory Approval: We can help provide the documentation support required for regulatory approval of your device or implant. In fact, Invibio has filed Device Master File and Drug Master File documents with the FDA. This can help you navigate through regulatory channels with greater efficiency and speed.
• Global Network of Resources: Invibio is such a good collaborator in part because we partner with other companies with specific expertise and capabilities. When counseling our clients, we invite these outside experts into the discussions. Our worldwide database of companies in testing, manufacturing, packaging and quality control has often proven invaluable to our clients in their search for the best products and the best ways to get them to market.

As an extra measure of support, we also regularly tap into the resources of our parent company, Victrex plc, a world-leader in the manufacturing of high-performance materials for industries as diverse as aerospace, food processing and health care.