We've built and run our own licensed site.
Guided by operators who've done it themselves.
What we do
ODC licence and permit applications prepared with you, right the first time, so you're not withdrawing and reapplying.
See packages → 02Design and build advice with inspection in mind, so you only build once.
See packages → 03Guidance on cultivation systems and operations from people who run a licensed site every day.
See packages → 04Guidance on GMP systems and inspection readiness from people running a GMP pharmaceutical manufacturing operation.
See packages → 05A straight read on whether a plan, site or deal stacks up, and operator-led training for your team.
See packages →Packages
Not sure where to start? Start with an Operator Strategy Session. Other engagements are scoped to your project. All prices in AUD, ex GST.
A board-ready plan: entry model, site, fit-and-proper readiness, capex/opex, fee schedule and timeline to first permit and GMP batch.
We prepare and manage your licence application with you, then support you through assessment and requests for information, with permit and inspection-readiness add-ons.
Monthly strategy session, priority access, ODC correspondence and variation support, permit calendar and quarterly compliance health check.
Independent operator review of URS, zoning and flows, security design, cultivation systems, commissioning and inspection readiness, alongside your architects and engineers.
A day on site at a fully licensed, operating facility for up to 4 attendees: operations walkthrough, build story, lessons-learned debrief, Q&A with the operators and a follow-up memo. Invitation only; vetted attendees. Travel extra.
The documented build journey: sequencing, timelines, budget vs actual, supplier and design lessons, templates and the mistakes register. Licensed to one entity under NDA.
Gap assessment, mock inspection and QMS build-out, guided by people running a long-established GMP pharmaceutical manufacturing operation.
2.5–3 hours with the operators, plus a written Operator Verdict memo within 5 business days. 100% credited to any larger engagement booked within 30 days.
Operator judgement at board level: board attendance, investor and capital-raise support, executive mentoring and crisis support.
A 1-day intensive, in person or online, plus templates, taught by active operators. Public cohorts capped at 20. In-house sessions available on request.
Why operators who consult
We did it the hard way: we went through ODC licensing, built fully licensed facilities, and we run them every day. We've also recently acquired a 31-year-old GMP pharmaceutical manufacturing arm, so we see the whole chain, from seed to GMP batch.
Real operators and consultants, with proven track records and fully licensed facilities up and running.
The unfiltered build story
We made decisions we'd make again, and some we'd never repeat. We hand that knowledge over candidly and in full, so you don't pay twice for lessons we've already learned.
How it works
Tell us about your company, your stage and what you're planning. We review every enquiry personally.
A candid 2.5–3 hour session with the operators, followed by a written Operator Verdict memo within 5 business days.
If it makes sense, we propose the right engagement. We advise, plan, review and train; you own and run your business. Your session fee is credited if you book within 30 days.
It depends on your site, model and funding, and that's the first thing we work through in a Strategy Session. One fixed point: the ODC needs a facility ready for inspection before it grants a permit.
No. The decision rests with the ODC delegate. We provide operator expertise to maximise application quality and readiness.
Yes, through a Facility Immersion Day. Attendees are vetted and escorted, no photos are permitted, and visit details are shared only after booking.
A quick 15-minute call to see where you're at and whether we're the right fit. Or book an Operator Strategy Session straight away. Prefer email? advisory@mvrise.com.au