Nitrosamines Risk Evaluation: deadline extended to Oct. 1st.
by PQE Group
As communicated by CMDh in their ‘information on nitrosamines for marketing authorization holders, published on HMA website1, the European Medicines Regulatory Network agreed to proceed with the extension of the Step 1 (risk evaluation) deadline of Nitrosamines impurities risk evaluation to October 1st, 2020.
Deadline extended due to covid-19 spreading.
The decision to extend the deadline to October 1st, originally scheduled on March 26th,
was taken after considering the reports on challenges encountered by several pharmaceutical companies trying to meet the original deadline, due to the severe restrictions put on by local authorities to fight the spreading of sars-cov-2, covid-19 disease.
EMRN encourages companies to complete Step 1 in advance, and take actions.
However, according to EMRN the deadline should not be considered as a reason to procrastinate Risk Evaluation, and generally the Nitrosamines risk containment: whenever possible, the European Medicines Regulatory network still encourages marketing authorization holders to complete the Step 1 and to submit the evaluation outcome before the extended deadline; for same reason, national authorities still should be as soon as nitrosamine impurities are found, and generally, marketing authorization holders should assess immediate risk to patients, and take necessary actions to avoid their exposure to Nitrosamines impurities with no delay.
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