Regulatory Compliance & Safety
Transparent documentation, research-only handling guidelines, and audit-ready controls for partners working with advanced compounds.
Regulatory alignment
Our operations follow stringent federal and state guidance to maintain full research-only compliance.
FDA & DSCSA
Supply chain integrity
Serialized lots, pedigree tracking, and electronic T3 documentation retained for 7 years.
DEA exemptions
Research use certification
Controlled substances excluded; buyers attest to institutional research use at checkout.
OSHA & DOT
Safety & transport
GHS-compliant labeling, SDS access, and UN3373 / UN1845 packaging as required.
Research use expectations
To safeguard both researchers and study integrity, we require the following from all clients.
Before ordering
- Institutional affiliation and lab manager contact on file.
- Research purpose statement provided during checkout.
- Agreement to indemnify against off-label or clinical use.
Upon delivery
- Inspect tamper seals and temperature indicators immediately.
- Store according to COA handling instructions within 30 minutes.
- Report any integrity concerns to compliance within 24 hours.
Onsite handling
- Restrict access to trained personnel with documented SOPs.
- Dispose of unused material via institutional hazardous waste programs.
- Maintain experiment logs and reference COA identifiers.
Audit & verification support
Need help preparing documentation for an internal audit or regulatory review? Our compliance desk can compile traceability packets within two business days.
- COA, SDS, and batch analytics consolidated in a single dossier.
- Signed statements of research-only distribution.
- Temperature log exports for cold-chain shipments.
Contact compliance
Reach the compliance desk directly for documentation copies, risk assessments, or escalation paths.
Research use only: We verify institutional credentials before fulfilling any order.