We raise the standard of what reaches your patient
Quality is not a promise — it is evidence. We only connect your clinic to compounding pharmacies that prove, batch by batch, the safety of their formulations.
What we require of every partner pharmacy
Good Practices (GMP)
Operation under Good Compounding and Manufacturing Practices, in line with Anvisa rules.
Current licenses
Proven sanitary regularity — Anvisa AFE/AE, sanitary license and fire-safety clearance (AVCB) — in a unified dossier.
Per-batch report
Potency, sterility test and bacterial endotoxins on every injectable batch produced.
Microbiological & physicochemical analyses
Every batch undergoes microbiological and physicochemical evaluations before release.
Qualified inputs
Raw materials from qualified suppliers, with traceability and a certificate of analysis.
Controlled environment
Sterile compounding in a controlled environment, under biosafety protocols.
Curation in four layers
Selection
We approve only pharmacies whose structure, licenses and track record fit sterile injectables.
Document verification
We check AFE/AE, licenses, fire-safety clearance and the report standard before approving the partner.
Per-order checking
On each order, we validate the formula’s fit and the availability of the batch report.
Traceability
We link batch, report and delivery, with a dossier available to your clinic for auditing.
Legal and clinical peace of mind, in writing
We provide a dossier that gathers the partners’ licenses and the per-batch microbiological report model. So before the first prescription, your team already has everything documented.
- Partners’ Anvisa (AFE/AE) and sanitary licenses
- Fire-safety clearance and controlled-environment evidence
- Per-batch report model (potency, sterility, endotoxins)
- Traceability from input to delivery
- Data and prescriptions handled under privacy law (LGPD)
Want to see our standard up close?
Request the sanitary dossier and a sample analysis report to review with your team.