XEVMPD (Article 57)

We can assist your organisation with the XEVMPD submissions, with training on SPOR, that will ultimately replace the XEVMPD. We will be there for you also when the ISO IDMP standards will be implemented in the EU. We can also assist you to complete and submit the Annex-I to the Risk Management Plan - Interface with EudraVigilance for Centrally Authorised Medicinal Products