Guidance for Industry, Third Parties and Food and Drug Administration Staff – Medical Device ISO 13485:2003 Voluntary Audit Report Submission Pilot Program (FDA 20123.19)
![](https://ecompliance.jp/wp-content/uploads/2006/09/ガイドライン-3.png)
https://qmsdoc.com/product/md-qms-358/
https://qmsdoc.com/product/md-qms-358/
株式会社イーコンプライアンス