EXTEDO Blog (6) | EXTEDO

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

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