WCRO provides global development services for medical device companies to facilitate an accelerated and seamless entry into the commercial market. Each year, we work with more than 100 companies from 10 different therapeutic and specialty areas whose regulatory pathways require all levels of FDA and CE approval. Our process culminates with reimbursement guidance and support to ensure these technologies are correctly and beneficially coded, as well as post market support to ensure the continued compliance and safety of your device. Our mission is to strive daily for the development of safe and effective technology using our experienced staff and extensive resources.Our clients represent the biggest names in healthcare: and industry; contact us and ensure you receive the best possible services for your research. Our team is equipped with top of the line equipment and software, and we are trained in the research of over 70 specialties. Whether you need minor editing for a clinical manuscript or a full statistical analysis of raw data, our trained staff is ready to assist.

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