Clinical governance
Who holds clinical responsibility, who reviews plans, and what happens when something goes wrong outside office hours. A clinic should answer these without hesitation.
Documentation you should leave with
If you cannot produce these afterwards, the plan was verbal, not clinical.
- A written plan naming compound, dose, route, and duration
- The monitoring schedule and what is being measured
- Stated risks, contraindications, and stopping criteria
- Who to contact, and how, if something changes
- Itemised costs across the full plan
Sourcing
Where applicable, preparations should come from a licensed compounding pharmacy against an individual prescription. Nothing on this page endorses any compound, pharmacy, device, manufacturer, or clinician. Descriptions are informational only.
Questions people ask about this
- What is the difference between a peptide clinic and a med spa?
- Branding differs more than the underlying requirement: a prescription needs a licensed prescriber and an individual evaluation regardless of the setting. Ask who that prescriber is.
- Should I get labs before starting?
- Where clinically indicated, yes. Reflexively ordering a large panel is not the same as ordering the labs relevant to your history and the proposed plan.
- Can I bring my own compound to a clinic?
- Most clinicians decline to administer material of unverified origin, because they cannot attest to its identity, purity, or sterility.
Where to go next
Prefer to talk it through? Call 214-718-1068 or email ac@dallasregenerativellc.com.