• End to end training on eCTD submission format to Health Canada (HC), US Food and Drug Administration (US FDA), Health Medicines Agency (HMA), European Medicines Agency (EMA) and Gulf Cooperation Council (GCC) including Saudi Food and Drug Authority (SFDA)
  • Training on setting up of gateway accounts and filing of eCTD submissions via the different gateways (ESG, CESG, CESP, WebClient)
  • Training on strategies and tips for a high quality eCTD output and regulatory document and dossier lifecycle management

2860, rue Lafrance Montréal, QC H4R 1H3

(+1) 514 623-4257