Biosafety & Research Compliance
Last reviewed: July 15, 2026
PeachBot Bio is an in-silico research, documentation, and decision-support platform. It is not a wet-lab system and must not be used to bypass biosafety, biosecurity, bioethics, institutional, national, or international controls.
1. In-Silico Only
PeachBot Bio supports computational analysis, literature organization, data structuring, education, governance review, and research planning. It does not provide, enable, or authorize biological synthesis, genetic engineering, organism modification, chemical synthesis, laboratory execution, clinical experimentation, field release, or procurement of controlled materials.
2. Prohibited Use
- Generating or optimizing wet-lab protocols, synthesis steps, pathogen manipulation, harmful biological activity, or evasion of safety controls.
- Creating, modifying, enhancing, releasing, or distributing organisms, biological agents, toxins, vectors, or genetic constructs without lawful approval.
- Bypassing institutional biosafety committees, ethics committees, regulatory permits, containment requirements, or professional supervision.
- Using outputs for dual-use, harmful, unlawful, unsafe, or environmentally irresponsible activity.
3. Institutional and Legal Oversight
Any downstream laboratory, clinical, agricultural, environmental, or field activity informed by PeachBot outputs must be independently reviewed by qualified personnel and approved through the relevant institution and authorities. Depending on jurisdiction and activity, this may include institutional biosafety committees, ethics committees, animal ethics committees, clinical review boards, environmental authorities, agriculture authorities, import-export controls, controlled-material rules, and funding-agency requirements.
4. Jurisdictional Awareness
- India: Consider DBT, ICMR, CDSCO, environmental, agricultural, institutional biosafety, clinical research, data protection, and ethics requirements where applicable.
- Singapore: Consider biosafety, biosecurity, research ethics, PDPA, healthcare, laboratory, and institutional governance requirements.
- UAE: Consider applicable health, environment, research, import-export, data protection, cybersecurity, and free-zone rules.
- EU/EEA: Consider GDPR, EU AI Act, biological safety, GMO, clinical research, medical-device, environmental, and member-state rules where relevant.
5. Responsible AI in Biology
PeachBot designs biological AI features with safety boundaries, restricted-use policies, human oversight, auditability, data provenance checks, misuse monitoring, and escalation paths. Relevant references may include ISO/IEC 42001 for AI management systems, ISO/IEC 23894 for AI risk management, ISO/IEC 27001 for information security, NIST AI RMF, institutional biosafety practices, and domain-specific ethical guidance.
6. No Replacement for Committees or Regulators
PeachBot does not replace biosafety committees, ethics boards, clinical investigators, principal investigators, regulatory authorities, legal counsel, laboratory directors, or environmental authorities. For research compliance questions, contact [email protected].