ISO 10993-11:2017 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
OBJAVLJEN
ISO 10993-11:2017
PROJEKAT
ISO/DIS 10993-11
40.60
Završetak javne rasprave
21. 6. 2025.
Biološko vrednovanje medicinskih sredstava – Deo 11: Ispitivanja sistemske toksičnosti
40.60 Završetak javne rasprave