Your Roadmap to Improving Lives

program_page_v2Cirtec brings three decades of experience in developing Class III medical devices fabricated under 21 CFR 820 and ISO 13485 quality standards. Our dedicated program management experts are here to help you bring your product from concept through commercialization – on schedule, on budget and as seamlessly and predictably as possible.

Whether you are an industry leading OEM or a cutting-edge start-up, Cirtec can develop and manage an integrated program that optimizes your technology for each successive step toward its clinical or regulatory build, and onward to commercial production.

We work closely with you to understand your requirements and provide you with a detailed, written statement of work that maps out the costs and timelines for your product’s entire development process. Once your project begins, Cirtec’s dedicated management teams work with you to ensure it meets every milestone.