Research Governance
Black Box Fields project documentation. Proposed plans are subject to site, funding, safety and regulatory verification.
Scientific design
Develop hypotheses, controls, data dictionaries, quality assurance, analysis plans, budgets and study-specific stop criteria.
Participant protection
Human-participant studies may require ethical review and informed consent; protect privacy and accessibility.
Records
Define permissions, secure storage, retention, backups, specimen identification and audit trails.
Authorizations
Controlled-substance research, possession or manufacture cannot begin without applicable DEA and other authorizations. An application is not approval.
Collaboration
Outreach to universities and laboratories is not an executed agreement; formal studies need documented responsibilities and permissions.
Get involved
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