We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » Quality Audits Will Assess Postmarket Needs in EU
Quality Audits Will Assess Postmarket Needs in EU
March 1, 2012
Devicemakers can expect quality system audits to include a review of their postmarket surveillance procedures, including plans for any required clinical follow-up studies, according to a new European Commission guideline.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor