Australia (TGA) Publishes First eCTD Guidance Documents
Australia has published their long-awaited eCTD guidance
- Guidance for Industry on Providing Regulatory Submissions for Prescription Medicines in Electronic Format (eCTD) in Australia
The AU M1 guidance bears a strong resemblance to EU Module 1 Specification.
I noticed a few interesting items in the Guidance for Industry:
- Section 4.1 allows for Word or RFT to be submitted in addition to PDF for general narrative documents (not just in M1 and M2). This is considered a review aid, but in this case both documents are stored together in the eCTD (presumably linked into the backbone), not stored separately outside the eCTD such as is the case with MS Word for M1 and M2 in EU. The AU guidance seems to imply that M1/M2 Word documents are stored outside the eCTD as in EU – it’s a little unclear as to whether these can be linked into the backbone.
- Section 4.4 includes a list of documents that must be text searchable, and a list of documents that do not need to be text searchable. To my knowledge, this has not been required in the past for eCTD, only for NeeS (with the possible exception of a few individual authorities in Europe). Some companies will need to update their procedures to OCR key documents – although of course it’s better to create them from MS Word source in the first place.