European regulators issue guidance on regulatory requirements in the context of COVID-19 pandemic
The European Commission, EMA and the European medicines regulatory network have developed a question-and-answer (Q&A) document to provide guidance to stakeholders on adaptations to the regulatory framework to address challenges arising from the COVID-19 pandemic, with a particular focus on crucial medicines for use in COVID-19 patients
European Regulators Issue Guidance COVID 19 | 13/04/2020 | By Darshana | 330
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