Quality System Inspection Support

Medical device and pharmaceutical company may face regulatory compliance / quality system review / inspection from regulatory authority, including routine review / inspection, fly inspection and For Cause inspections, etc.


Our Services:

Daily complaince consulting

Review IFU and labels

Review design change

Assist in voluntary recall

Submit medical device reports to the FDA

FDA Inspection Observations Form 483 reply and warning letter close

QMS targeted training


Copyright©www.mid-link.net,All rights reserved.
检验检测·法规咨询·质量体系·CDMO·医学检验
400 821 7661    sales@mid-link.net
天津市经济技术开发区第九大街51号融达科技园B座一层
XML 地图