eCTD transmissions | Australia

ASPHALION and our partner Extedo® can guide you with Australian submissions. We can support you in a variety of activities.

ASPHALION and our partner Extedo® can guide you with Australian submissions. We can support you in a variety of activities.
January 21, 2022

From 1 November, 2021, the Australian Therapeutic Goods Administration (TGA) begins a staged transition to Electronic Common Technical Document- only for all prescription medicines.

Stage 1 of the transition to eCTD-only has just started for all regulatory submissions in Australia. From this date, the following drug applications must be submitted to the Therapeutic Goods Administration (TGA) using the eCTD:

  • New Chemical Entity Medicine (Type A)
  • New Biological Entity Medicine (Type A)
  • New Biosimilar Medicine (Type A)
  • New Combination Medicine (Type B)

Although the majority of the applications of stage 1 are already provided to TGA within eCTD format, requests for exemptions will be assessed by the TGA on a case-by-case basis.

Have a look at the document here: ASPHALION EXTEDO AUSTRALIA eCTD TRANSMISSIONS

For further information you can contact us at: ectd@asphalion.com

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