ODC Medicinal Cannabis Permit Holder Supply Pathways 2026 - Page 1 of 4 - Therapeutic Goods Administration

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1. What medicinal cannabis permits do you hold?

Cultivation and Production Manufacture only Cultivation, Production and Manufacture

2. Which of the following supply pathways do you use to supply cannabis, cannabis resin (including rosin) and other cannabis drugs? Select all that apply

Transfer to your own ODC medicinal cannabis manufacture licence Supply to another ODC medicinal cannabis licence holder authorised to manufacture Supply to a GMP authorised manufacturer Supply to a Commonwealth, State or Territory authorised research or testing entity Supply to an authorised waste disposal/destruction entity Supply for extemporaneous compounding Supply to a public hospital pharmacy Supply for use in a clinical trial Export (under valid export licence/permit) Other (please specify)

3. Which of the following supply pathways do you use to obtain cannabis or cannabis resin (including rosin) and other cannabis drugs? Select all that apply

From your own medicinal cannabis cultivation and production licence From another ODC medicinal cannabis licence holder authorised to cultivate and produce From a State or Territory licence holder Imported (under a valid licence/permit) N/A Other or further detail

4. In the past 12 months, what percentage of your total permitted quantity of cannabis material (dry weight, with 10% moisture content) did you produce, compared to the quantity authorised?

0-20% 21-40% 41-60% 61-80% 81-100%

5. During the past 12 months, approximately what proportion of your total production is allocated to the following: Provide percentages – total should equal 100% Please answer in text box below.

6. What is the typical storage duration for product (excluding waste) prior to supply?

Less than 1 month 1-3 months 3-6 months 6-9 months 9-12 months Greater than 12 months

7. In the past 12 months, have you been required to destroy product intended for supply?

Yes (Specify below) No N/A