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