Global Peptide Compliance Advisory

I am preparing to sell research-grade peptides and related bioregulators and need solid, practical guidance to ensure full compliance with regulations worldwide. My key focus is regulatory compliance; I am not looking for contract drafting or IP work at this stage.

What I need from you
• A clear map of the governing bodies that regulate peptides in the United States (FDA, DEA, state boards), European Union (EMA, customs), Australia (TGA, customs) and any other major markets we identify together.
• An analysis of how these agencies currently classify peptides and bioregulators, including the grey areas that often trigger enforcement.
• Step-by-step guidance on what I can legally say on my website, labels and marketing materials, plus any required disclaimers for a “research only – not for human use” positioning.
• Import / export do’s and don’ts: paperwork, permits, record-keeping and red-flag countries.
• A concise checklist I can hand to my fulfillment team so every shipment stays compliant.

Acceptance criteria
Your final deliverable will be a written memorandum (PDF or DOCX) that addresses each of the bullet points above, cites the relevant statutes or guidance documents, and highlights practical action items I can implement immediately. A short Q&A call (30-45 min) to walk me through the key points will mark project completion.

If you have direct experience advising peptide or SARMs vendors, or you have handled cases involving bioregulators, please mention it when you bid.