27 March 2026
Festina Lente Down Under: What Australia Is Teaching the World About Legal Psychedelic Therapy
By: Jamarie Geller, MD, MA
MAPS Bulletin: Volume XXXVI

How Are We Going?
I realized after a few moments that the flight attendant’s question was not in reference to the aircraft I was boarding, but the Australian “how are you?” As a psychiatrist and psychotherapist with experience in psychedelic medicine who spent many weeks exploring the psychedelic landscape of this magnificent country, the question started to land more existentially than casually. How was my trip through this life getting on, since what began as a chance encounter at Psychedelic Science 2025 and a quest to help with international psychedelic research became an inquiry into Australia’s psychedelic ecosystem? Where a remarkable proportion of the country’s flora and fauna exist nowhere else on Earth (see: Quokkas), Australia is also home to a growing number of psychiatrists, therapists, clinics, and researchers working in an environment where MDMA- and psilocybin-assisted therapy (broadly, psychedelic-assisted therapy or PAT) are permitted for specific psychiatric indications—legally, on the national level.
While the United States has actively and empirically pursued answers in this (re)emerging field, it has been constrained by both political and legal realities in its ability to study what happens when PAT is integrated into real systems with real-world complexity. While Australia does not have all the answers either, over the past two years, clinicians and researchers there have amassed hard-earned, experiential knowledge navigating legal psychedelic care, and leveraging this collective wisdom is more important than ever.
Studying and governing PAT, and then delivering safe, inclusive, equitable, and effective care using such complex therapies requires collaboration across disciplines, institutions, and borders. To this end, I spoke with researchers, clinicians, community members, and other stakeholders—nondirectively, of course—across the globe from my American home, aiming to be a part of this global knowledge and subsequently sharing insights when possible.
A Bold Decision with a Careful Rollout
In 2023, Australia’s Therapeutic Goods Administration (TGA), the country’s FDA-equivalent, reclassified MDMA and psilocybin, permitting their use alongside psychotherapy for posttraumatic stress disorder (PTSD) and treatment-resistant depression (TRD), respectively. The decision surprised many, including some who had long advocated for expanded research but did not expect regulatory approval to arrive so abruptly.
The pace of adoption since then has been slow. As of December 2025, data released through a Freedom of Information request indicate that 123 patients had received MDMA-assisted therapy (MDMA-AT) and 65 received psilocybin-assisted psychotherapy (PAP) under this framework (TGA, 2026). Psychiatrists are currently the only professionals permitted to prescribe these substances, and before offering PAT, they must obtain approval through what is known as the TGA’s Authorized Prescriber (AP) scheme as well as a Human Research Ethics Committee. The process often takes a year or more, leading many psychiatrists to seek support from specialized consultancies with expertise in both regulatory navigation and clinical protocol development.
Once approved, the APs assume responsibility for assembling and overseeing the treatment team, including psychotherapists, and remain ultimately accountable for patient safety and the integrity of the process. To date, there remain relatively few APs, with fewer than 50 nationwide (including 48 authorized to prescribe MDMA and 40 for psilocybin).
There is also variation in regulation on the state level, which is ever-evolving, and has led to some additional barriers to access and confusion for clinicians. While the TGA sets federal scheduling and prescribing conditions, states retain authority over implementation.
Early Themes from the Field
While no one I spoke with claimed that Australia had all the answers, several important themes emerged.
Rollout and Access Concerns
There was near consensus that the TGA’s approval of MDMA-assisted therapy for PTSD and psilocybin-assisted therapy for TRD was both unexpected, and perceived by some as precipitous. Concerns have been raised, though, both about the rapid regulatory U-turn and about the glacial pace of adoption. Several factors have contributed to this slow uptake, including the high cost of treatment, restrictions on direct-to-consumer marketing, and a complex approval process for APs and clinics.
Until recently, there was no insurance coverage for PAT, and the cost of a standard course of care, including screening, preparation, dosing, and integration, has typically ranged from 20,000 to 30,000 AUD (13,000-20,000 USD). The TGA currently requires two therapists in each dosing session for all PAT, which some cite as appropriate given the way at least MDMA-assisted therapy has been studied, but others believe this requirement unduly raises cost to patients. However, in mid-2025, Medibank, Australia’s largest private health insurer, announced coverage for PAT through a partnership with a psychedelic service provider. In November, 2025, the Australian Department of Veterans’ Affairs also signaled plans to start coverage for eligible veterans. Although these developments are expected to expand access, affordability and equity are ongoing issues.
Many clinicians expressed difficulty navigating national regulations as they sought AP status and sought to expand clinical services at their hospital or clinic to include this kind of treatment safely and lawfully. Providers are required to submit detailed protocols outlining their therapeutic model and safety procedures. If they are approved and begin to provide PAT, however, there is relatively little systematic follow-up beyond safety reporting to assess adherence, provide ongoing support, or facilitate shared learning across sites, compounding jurisdictional variation.
I also heard concerns from clinicians and other community members about the absence of Aboriginal and Torres Strait Islander peoples in initial and some ongoing discussions, which is especially salient given the history of Australian colonization, the use of these kinds of medicines in indigenous communities, and the urgent need to address generational and ongoing trauma. These communities have largely been excluded from both participating as facilitators and accessing treatment due to cost, regulations, and trying to fit PAT into colonial diagnostic and healthcare structures (Bianca, 2024). Across Australia, I heard understandable calls to address these injustices by consulting Aboriginal and Torres Strait Islander people in regulatory decision-making, supporting diversity in training, on treatment teams, and in research, and for increasing access.
Even with regulations in place, many clinicians expressed lingering concerns about clarity–around training standards, oversight mechanisms, and how emerging challenges will be addressed as experience accumulates. Dr. Nigel Strauss, MD, one of the country’s first APs and an ardent supporter of PAT, is discouraged by the lack of leadership by the Royal Australian and New Zealand College of Psychiatrists (RANZCP) and other professional groups. He informed me that the RANZCP psychedelic steering committee, on which he once sat, has in fact officially been disbanded. He expressed concerns about the overall lack of psychedelic knowledge amongst providers, and worries that the right experts are not being consulted.
Additionally, due to strict restrictions on direct-to-consumer marketing and broad cultural differences, many Australians are also not aware of PAT. Many still lack a basic understanding of psychedelic medicine, don’t know that it may be available to them, nor how to find it.
Scaling: Training, Workforce, and (Clinical) Expansion
Everyone in the psychedelic space agrees that quality of care is foundational, but balancing safety and workforce expansion to meet access needs can be a challenge. In the United States, as psychedelics selectively become decriminalized and approved by some states for clinical use, there is much discussion about how to certify medical providers and therapists involved in the provision of psychedelic treatments. In Australia, professional eligibility for physicians is relatively clearly defined: psychiatrists assess the patient and prescribe, and therapists deliver much of the preparation, dosing support, and integration under psychiatric oversight (and, in some cases, the psychiatrist engages in the provision of psychotherapy themselves). It is less clear what constitutes sufficient training to provide psychedelic-assisted therapy well. Dr. Strauss stressed the importance of specialized training in both PAT and experience with TRD, PTSD treatment, and crisis response to ensure safety and efficacy.
There are now multiple training programs of varying length, depth, and orientation, but there is no national accreditation or certification process to establish readiness, resulting in wide variability in therapist preparation. This has raised concerns about ethical practice, consistency of care, and a risk of adverse events, particularly in the absence of centralized oversight or peer and other support structures. At the same time, restrictions on who may serve as a therapist have excluded many experienced psychotherapists whose training and clinical orientation may be well-suited to this work.
Practical barriers to expansion extend beyond workforce limitations, but the sourcing of psychedelic medicines themselves is becoming easier and more localized, with three approved suppliers, including one based in Australia.
Patient selection, psychological flexibility, social support, and readiness for non-ordinary states of consciousness emerged as critical considerations in general when considering PAT. The need and suggestions to taper antidepressants prior to MDMA and psilocybin treatment, respectively, have also posed challenges, sometimes destabilizing patients who otherwise might benefit (although tapering is up to provider’s discretion and may not be universally applied). These issues will need to be considered as these early models grow.
Optimizing treatment models on a small scale to meet the needs of the community delivered by the earliest operational clinics seems to have served Australia well, but how the psychedelic medicine community will expand services for Australian citizens more broadly is an open question. Some worry about how the quality of this type of specialized, and ideally highly personalized treatment modality will fare when scaled, but others are justifiably concerned about the apparent lack of access and financial realities involved in providing psychedelic services.
Data, Learning, and the Absence of Centrality
Legal realities have created a vacuum of real-world data available about MDMA-AT and PAT, but where these novel treatments are already in use, there is a trove of important and highly useful information that grows with each additional patient. The current framework includes some centralized data collection, including adverse events through the TGA, which as of December 2025 reported zero events under the Authorised Prescriber scheme since July 2023 (TGA, 2026). However, data reporting remains limited in scope and is not yet integrated into a comprehensive, transparent system for evaluating outcomes, adherence, shared learning, or developing best practices across sites.
While a national data registry has also been launched, treatment sites are not required to submit their data; therefore, learning is largely anecdotal and siloed, and organized information about efficacy and safety, as well as systems-level factors that influence outcomes, is not available. Without requirements or willingness to utilize a shared infrastructure for data aggregation and analysis, much of this knowledge is at risk of being lost at a time when we need it most. One provider suggested a nationwide patient-led tracking system, citing systemization and cost benefits. I am biased toward data collection and sharing generally, but in this situation, Australia is clearly missing the opportunity to contribute to the shaping of psychedelic medicine into a more evidence-informed field via the gathering of real-world outcome data.
Lessons Beyond Australia
There is much the global psychedelic community can learn from Australia’s experiment.
First, training and oversight matter, but they must be designed to ensure quality without creating insurmountable bottlenecks. As other countries and jurisdictions consider liberalization of drug laws and regulatory approval for clinical use, it will be important to think up front not just about what professional degree is needed, but also who will provide consistent, quality training, and which regulatory bodies will oversee credentialing and quality-assurance. This requires thoughtful preparation with anticipation of challenges, including those we have seen reflected in Australia’s process.
Second, access and equity must be addressed early, including for First Nations/Indigenous populations, particularly as costs remain high and reimbursement is limited. Third, real-world data collection should be prioritized from the outset, with mechanisms for transparent sharing of both successes and challenges, including broader public health outcomes, healthcare utility, and associated financial impact.
Perhaps most importantly, international collaboration is essential. Given the scale of unmet need for effective treatments for depression, trauma, and a number of other domains of human suffering, no single country can afford to learn in isolation. Centralizing elements of governance, training standards, and data infrastructure, while allowing for local adaptation, may help accelerate learning while preserving safety, efficacy, and clinician and community autonomy.
As Dr. Strauss wisely suggests: Festina lente, meaning “make haste slowly.” Australia’s cautious pacing – informed by clinician and community feedback – appears to have served the country well so far, albeit with a limited population. If the global community can learn from each other by sharing insights while honoring the specific needs of different cultures and groups, we may be able to move both more quickly and more wisely – “going” better, together.
Acknowledgements
It is also incumbent on me to express the utmost gratitude. Many, many people made this piece possible. Thank you. I was humbled on this quest through Australia, literally every day, by the generosity, hospitality, trust, and collaborative spirit I encountered over and again, meeting fantastic clinicians, thoughtful researchers, and many other busy professionals who opened their homes, their towns, and their hearts to a stranger in a strange land.
I wish to specifically thank Empax Centre, Nigel Strauss, Joanne Shannon, Agnieska Sekula, Voytek Bereza, Scott Shannon, Joe Starke, Anthony Bloch, Ariana Elias, Daniel Roberts, Indigenous Psychedelic-Assisted Therapies (IPAT), Laura Nissley, Ruth Schekter, Bill Zirinsky, other clinicians and community members who shared their time and perspectives, and others in the community in the US and abroad who supported my journey in many ways to bridge the international divide.
I also want to thank Chris Raine and The Psychedelic Consultancy for facilitating introductions and conversations during this reporting.
This article reflects conversations with a wide range of Australian clinicians, researchers, and community members; interpretations and any errors are my own.
References
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Jamarie Geller, MD, MA
Jamarie Geller, MD, MA, is an integrative child, adolescent, and adult psychiatrist and psychotherapist practicing in Colorado and Michigan. She has a Master’s in contemplative psychotherapy and is adjunct clinical faculty at the University of Michigan. Her work focuses on community and collaboration, integrating traditional, contemplative, trauma-informed, systems-based, and psychedelic approaches to care. She is especially interested in relational and deep healing, which guides her clinical work and research with ketamine, psychedelics, and empathogens.

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