Professional & Institutional Inquiries
Not By Chance Life LLC supports licensed medical professionals, institutional operators, and qualified research entities through structured regulatory education and credential-based documentation access coordination within the 21 CFR Part 1271 Section 361 framework.
Category overviews are available within the Biologic Product Portfolio .
This page is intended exclusively for professional and institutional inquiries. Consumer inquiries are not supported.
Before Submitting an Inquiry
Professionals seeking documentation transparency or supplier evaluation clarification are encouraged to review the Structured Supplier Evaluation Process prior to contacting our office.
Foundational regulatory context is available within our Peer-Reviewed Scientific References .
Provider Access Requests
Licensed healthcare providers seeking access to supplier documentation must initiate credential verification through the Provider Credential Verification Portal .
Credential review is conducted manually prior to documentation release. Access is not granted via general email inquiry.
Professional Access & Communication Standards
The reference below outlines eligibility criteria, communication discipline standards, and structured inquiry procedures associated with Not By Chance Life LLC.
Appropriate Institutional Inquiry Categories
- Regulatory framework clarification
- Institutional onboarding discussions
- Multi-location governance coordination
- Documentation and traceability review alignment
- Professional partnership discussions
Professional Communication Channel
Institutional inquiries may be directed to:
Email: info@notbychance.life
Please include:
- Full name
- Professional designation
- Institution or organizational affiliation
- Nature of inquiry
Credential verification requests must be submitted exclusively via the Provider Credential Verification Portal and are not processed through general email.
Defined Organizational Role
Not By Chance Life LLC functions solely as a regulatory education and documentation coordination entity.
We do not:
- Provide medical advice
- Recommend treatment protocols
- Participate in clinical decision-making
- Manufacture, process, store, or ship biologic materials
All manufacturing, laboratory testing, donor screening, and fulfillment are performed directly by Regenerative Research Group (RRG).
Governance structure details are outlined in our Governance & Compliance Policy .
Regulatory & Compliance Notice
Certain referenced materials may be regulated as Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps) under 21 CFR Part 1271 Section 361.
Registration under 21 CFR Part 1271 does not constitute FDA approval, clearance, endorsement, or evaluation of safety or effectiveness.
These materials have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease.

