Home > Newsletters > International Medical Device Regulatory Monitor > Report: PIP Case Highlights MHRA’s Need for More, Better Medical Device Data
International Medical Device Regulatory Monitor
June 2012 | Vol. 20 No. 6
Report: PIP Case Highlights MHRA’s Need for More, Better Medical Device Data
While judging the Medicines and Healthcare products Regulatory Agency’s (MHRA) response to the PIP silicone breast implant scandal basically sound, a new review by the UK Department of Health (DOH) finds the agency needs better access to information on devices to preclude similar safety scares in the future.
ePublishing :: CMS, Hosting & Web Development | © Copyright by FDAnewsAll rights reserved. Do not duplicate or redistribute in any form.