Mid-Link Group is a leading firm in providing medical device and pharmaceutical regulatory consulting and testing service. We have our own consulting team in both China and north America, and a 40,000 square-feet testing laboratory with ISO 17025 accreditation and compliance to FDA GLP. We provide our value clients a one-stop service from product development to post-market follow-up, from testing (Bench testing, pre-clinical testing and usability/human factor evaluation) to global pre-market registration, and from internal quality system audit to supplier audit. It is always our target to provide professional, timely, and efficient services.