Therapeutic Goods Administration (Australia) to transition all regulatory submissions to eCTD-only, starting in 2021
MHRA Publishes New Guidance for Converting Centrally Authorized Products to UK Marketing Authorizations
EXTEDO Expands its Global Reach in Pakistan
EXTEDO Adds Comprehensive Cloud-Based Document Management System To Their Portfolio
EXTEDOpulse - Synergy, Connection and Innovation
Taiwan FDA Chooses EXTEDO’s Solutions For Validation & Reviewing
Free of charge usage of the EXTEDO eLearning platform for EXTEDO customers until 30 June 2020
EXTEDO & Wrike announce strategic partnership to release a planning and tracking solution for the life sciences industry
EU IDMP Implementation Guide Version 1 Released
EXTEDO Innovation Days & User Group Meetings replaced by virtual meetings
COVID-19 Update
eCTDmanager Generated Valid EAEU Test Submission