Turn the idea into a funded, reviewable proposal in 90 days
Illustrative planning schedule · Research starts only after approvals. Days 1–30: verify the sponsor's resources and governance, appoint Philippine and US legal and scientific advisers, review current rules, and publish an evidence map. Choose one clinical question and identify an academic host. The deliverable is a bounded cannabis concept with a preliminary permission map, not a recruitment announcement or a promise of government acceptance.
Illustrative planning schedule · Research starts only after approvals. This page expands the “Turn the idea into a funded, reviewable proposal in 90 days” chapter in the cannabis collection.
Days 1–30: verify the sponsor's resources and governance, appoint Philippine and US legal and scientific advisers, review current rules, and publish an evidence map. Choose one clinical question and identify an academic host. The deliverable is a bounded cannabis concept with a preliminary permission map, not a recruitment announcement or a promise of government acceptance.
Days 31–60: obtain partner capability assessments and real cost estimates, seek regulatory consultations, and draft a research concept, consent approach, privacy plan, safety arrangements, and publication terms. Cost personnel, facilities, lawful supply, analysis, oversight, injury coverage, and the capacity to repeat unsuccessful work. Keep advocacy and research budgets distinguishable.
Days 61–90: complete a costed Philippine–USA proposal for institutional review and the applicable regulatory submissions. Define decision gates for lawful feasibility, product quality, scientific value, funding sufficiency, ethics, and safety. Later clinical work depends on approvals and readiness, not this calendar. Publish a proceed, revise, or stop decision with reasons, then evaluate any policy expansion separately.
Open this exact section in the Necromancer dossier. The original chapter status is “Illustrative planning schedule · Research starts only after approvals.”
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