Electronic product information (ePI) by E. Scanlan (EMA)
Revision of QRD template for package leaflet (PL) improvement
QRD Template #QRD #template #pharmaceutical
EMA templates and EU terminology for medical translators - the Basics
EMA workshop on patient experience data in medicines development and regulatory decision-making
EMA IRIS Inspections Industry training on GMP & GCP
EU Marketing Authorisation | What are the Steps and Timelines for Centralised Procedure at EMA?| DRA
Information Workshop on electronic Product Information (ePI)
How to Best Prepare for an EMA Policy 0070 Submission
EMA templates and EU terminology for medical translators - Beyond the Basics
Translation Memory for European Medicines Agency QRD Template 10.1 English German
CIS Template Based BOM App Overview
Clinical Data Publication (Policy 0070) re-launch - EMA webinar
Streamlining Operations With Practice Management from ModMed®
EMA webinar on Article 117 of the Medical Devices Regulation EU 2017/745
eCTDtemplates - EXTEDO's eCTD Word Templates for FDA, EMA, Health Canada, EAEU, and Asia
EMA Account Management
Regulatory Reliance Tools Unveiled: A Practical Guide by EMA
EMA Account Management training webinar
EMA Veterinary Info Day on 13 May 2022
