Issuing documents during lockdown
In this unprecedented time of lock down, and with most notarial offices – and indeed the Foreign and Commonwealth Office legalisation desk – are closed.
Some important documents are still being processed for example: –
- The European Medicines Agency (EMA). The EMA is responsible for the scientific evaluation of centralised marketing authorisation applications(MAA). An application may be made to a European regulatory authority for approval to market a medicine within the European Union. Once granted by the European Commission, the approval to market a medicine in one, several or all European Union Member States is valid in all European Union (EU) Member States, Iceland, Norway and Liechtenstein.
- Medicines & Healthcare products Regulatory Agency (MHRA)