{"id":279723,"date":"2024-10-19T18:53:09","date_gmt":"2024-10-19T18:53:09","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bsi-19-30376763-dc\/"},"modified":"2024-10-25T15:27:30","modified_gmt":"2024-10-25T15:27:30","slug":"bsi-19-30376763-dc","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bsi-19-30376763-dc\/","title":{"rendered":"BSI 19\/30376763 DC"},"content":{"rendered":"

This document specifies requirements and gives guidance on the procedures to be followed in the preparation of samples and the selection of reference materials for medical device testing in biological test systems onlyin accordance with one or more parts of ISO 10993<\/span><\/span>. Specifically, this document addresses the following:<\/p>\n