QbD Group
    Regulatory Update

    New Update of Appendix 1 of the Nitrosamines Guideline

    On 04/07/2024, the European Medicines Agency (EMA) released an update to Appendix 1 (EMA/154403/2024 /Rev. 5) of the Nitrosamines Guideline. In this Appendix the different nitrosamines that have an established Acceptable Intake (AI) are listed.

    2024年7月9日2 分钟阅读

    What’s new?

    In this update, the Acceptable Intake (AI) values for nitrosamines related to the use of DIPEA (NDIPA and NEIPA) and NMP (NMBA) have been re-evaluated according to CPCA standards, resulting in a notable increase. Additionally, new nitrosamine drug substance-related impurities (NDSRIs) associated with the manufacturing processes of several active substances (Cinnarizine, Benzydamine, Bilastine, Caspofungin, Riociguat, Clarithromycin, Tramadol, Valsartan, Dimenhydrinate/Diphenhydramine, Tigecycline, and Trandolapril) have been published.

    Updates of the AI values have also been made to other NDSRIs, such as Nitroso-STG-19 from Sitagliptin and N-nitroso-desmethyl-citalopram. Furthermore, the nitrosamine 1-(2,3-dichlorophenyl)-4-nitrosopiperazine, previously incorrectly linked to Eculizumab, is now correctly associated with Aripiprazole. The CPCA category of N-nitroso-N-desmethyl-dextromethorphan has also been corrected.

    What does this mean to you?

    This update significantly impacts the assessment of nitrosamines related to certain solvents (NDIPA, NEIPA, and NMBA). With their AI values notably increased, the acceptable limits of these impurities have also risen. This change means that some assessments could shift from a risk to no risk conclusion. Moreover, the specification limits for these nitrosamines are now higher.

    If you market medicines containing any of the active substances listed above, you should review whether you have assessed the potential presence of these new NDSRIs. If not, it’s crucial to promptly update your NRA to consider these new risks.

    For those who have already assessed these NDSRIs and identified a risk, the next step is to verify whether the AI values used in your calculations have changed with this update. The limits may have changed significantly, potentially altering the conclusions of your confirmatory analysis results.

    How can QbD Group assist you?

    Our expert team toxicologist is here to guide you through regulatory changes and ensure your Nitrosamine Risk Assessments are up-to-date and compliant.

    关于作者

    Pablo Palomar
    Pablo Palomar

    Senior Toxicology Officer

    Regulatory Affairs services

    Navigate Regulatory Complexity with Confidence

    Navigate complex regulatory landscapes with expert guidance across pharmaceuticals, medical devices, and IVD.

    Read more
    分享本文

    订阅生命科学领域的最新动态

    专家观点直达您的收件箱——选择您的兴趣。

    绝无垃圾邮件。随时取消订阅。

    继续阅读

    相关内容

    我们使用 Cookie 来改善您的体验

    我们使用必要的 Cookie 来保证网站功能,以及可选的分析 Cookie 来改善我们的服务。 阅读我们的 隐私政策Cookie 政策.