Compliance Dashboard
FDA, FTC, PCAC, and 503A compliance posture across the platform.
High Priority
CMP-01
NA Bioscience FDA 510 Registration Verification
Compliance attorney must verify API manufacturer registration before routing into 503A channel.
Due
Jul 01, 2026
Action RequiredJul 01, 2026
CMP-02
Adverse Event Reporting SOP
Drafting SOP for clinic-reported AEs across all peptide products.
Due
Jul 10, 2026
In ProgressJul 10, 2026
CMP-03
Marketing Claim Review — All Materials
FDA/FTC review of every clinic-facing marketing asset before distribution.
Due
Jul 15, 2026
In ProgressJul 15, 2026
CMP-04
PCAC Meeting Monitoring
BPC-157, TB-500, MOTS-C, Semax, KPV — live monitor day-of.
Due
Jul 23–24, 2026
ScheduledJul 23–24, 2026
Standard
CMP-05
State Pharmacy Licensure Audit
Confirm 50-state coverage of Empower; gap-fill via Massey/NDL.
Due
Aug 01, 2026
In ProgressAug 01, 2026
CMP-06
Patient-Specific Rx Verification Workflow
Implemented across all active clinics.
Due
May 30, 2026
CompleteMay 30, 2026
CMP-07
503A vs 503B Channel Documentation
Routing rules documented for each product.
Due
Jun 01, 2026
CompleteJun 01, 2026
CMP-08
HIPAA Business Associate Agreements
BAAs with each pharmacy partner.
Due
Jul 30, 2026
In ProgressJul 30, 2026
CMP-09
GHK-Cu Non-Injectable Category 1 Filing
Filed post-FDA restoration.
Due
May 14, 2026
CompleteMay 14, 2026
CMP-10
Annual Compliance Training — All Staff
Schedule Q3 training.
Due
Sep 01, 2026
PendingSep 01, 2026
