EU Says Nitrosamine Risk Info Also Needed For New Drug Filings

Incomplete Info May Impact Granting Of Marketing Authorization

Companies seeking approval of new drugs must provide information on nitrosamine-related risk evaluation either as part of their marketing application or during the evaluation process.

Research analyst adding reagent to drug to keep tracking chemical reaction - Image
EU Has Updated Guidance On Nitrosamine Risk Evaluations • Source: Shutterstock

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