• How are regulators addressing Schedule I substance reclassification?
• What clinician certification requirements are emerging?
• How do payer coverage policies differ for psychedelic vs traditional therapies?
• What IP protection strategies work for natural psychedelic compounds?
• How are treatment centers managing liability insurance?
• What patient screening protocols prevent adverse events?
• How are real-world evidence platforms capturing long-term outcomes?
• What lessons can be drawn from cannabis legalization?
• How are investors assessing commercialization timelines?
• What role do patient advocacy groups play in destigmatization?
• How are integration therapies being standardized?
• What manufacturing challenges exist for GMP psychedelics?

• Psychedelic-Assisted Therapy
• FDA Breakthrough Designation
• Treatment-Resistant Depression
• Risk Evaluation
• Clinician Training
• Insurance Coverage
• Patent Strategies
• Dosing Protocols
• Long-Term Efficacy
• Stigma Reduction
• Clinical Trial Design
• IP Protection

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