Clinical Trials can be long and expensive. We bring a 360° experience of the wound care market to the choice of objectives, study design and implementation to deliver good quality and commercially relevant evidence.
International Regulatory experience and comprehensive strategic thinking applied to your product design, prototype and regulatory pathway.
A Medical device sold in Europe, irrespective of its classification, must have an up-to date Clinical Evaluation Report (CER) as part of its technical file. Wound Market Consulting can support, compile and provide expert advice to ensure compliance against the necessary requirements.
Monitoring and managing clinical trials is complex, requiring rigorous attention to detail, and a dynamic problem-solving approach. Partnering with Wound Market consulting will provide you with access to industry experts and a project team specialised in wound care.