GMP topical

12.07.2024

EMA: Updated Appendix 1 of the Nitrosamine Q&As

EMA: Updated Appendix 1 of the Nitrosamine Q&As

The European Medicines Agency (EMA) updated Appendix 1 (EMA/307633/2024 /Rev. 5) of the Nitrosamine Q&As, listing nitrosamines with established Acceptable Intake (AI) values.


The update includes re-evaluated AI values for nitrosamines related to DIPEA (N,N-diisopropylethylamine) (NDIPA (N-nitrosodiisopropylamine) and NEIPA (N-nitrosoethylisopropylamine)) and NMP (N-methyl pyrrolidinone) (NMBA (N-Nitrosomethylaminobutyric Acid)) according to CPCA (carcinogenic potency categorisation approach) standards, resulting in significant increases. Additionally, new nitrosamine drug substance-related impurities (NDSRIs) associated with the manufacturing processes of several active substances have been added (e.g. Cinnarizine, Clarithromycin, Tramadol, Valsartan).

Updates to AI values have also been made for other NDSRIs, such as Nitroso-STG-19 from Sitagliptin and N-nitroso-desmethyl-citalopram, and some other corrections have been made.


Source:

EMA: Nitrosamine impurities


 

Comments


I want the final date of Step-2 data submission of nitrosamine impurity of Eu for any product
dattatray bankar 10.09.2024
> Do not hesitate, we look forward to your feedback!