Creo Quality, headquartered in Central Indiana, was established in 2006 to assist medical device companies, particularly start-up and smaller companies, with product development, FDA quality system regulations, and project management needs. Over the years, we have grown and evolved as experts in FDA design controls and FDA and regulatory submissions, such as 510(k) and CE technical files. With this expertise, we have earned a proven track record in taking medical device product ideas from concept to market. We also specialize in project management direction which includes setting the proper timelines and budgets in order to meet your goals.
For years we have strived to help ideas get to market and believe that having a strong network of dependable sources to rely on is the best way to do this. Therefore, we have put together a powerful association of life science resources, partners, and suppliers in Indiana that can be utilized to help you meet your needs.
Creo Quality is committed to providing strategic solutions that address the entire needs of an organization rather than just individual projects, thus improving your chances for success.