{"id":282594,"date":"2024-10-19T19:06:17","date_gmt":"2024-10-19T19:06:17","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bsi-20-30381874-dc\/"},"modified":"2024-10-25T15:49:27","modified_gmt":"2024-10-25T15:49:27","slug":"bsi-20-30381874-dc","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bsi-20-30381874-dc\/","title":{"rendered":"BSI 20\/30381874 DC"},"content":{"rendered":"

This document specifies requirements and test methods for Needle-Based Injection Systems (NISs) for single-patient use intended to deliver discrete volumes (bolus) of medicinal product, through needles or soft cannulas for intradermal, subcutaneous and\/or intramuscular delivery, incorporating pre-filled or user-filled, replaceable or non-replaceable containers.<\/p>\n

Stand-alone prefilled syringes defined by ISO 11040-8<\/span><\/span> are not covered by this document (see exclusions below). However, when the prefilled syringes are provided to the user with an integrated addition, certain portions of the ISO 11608 series<\/span><\/span> apply as follows:<\/p>\n