About
CRE8 Pharmacy is a compounding pharmacy that creates personalized medications tailored to individual patient needs. Rather than dispensing mass-produced pharmaceuticals, they formulate custom medications for patients who require specific dosages, need to avoid particular inactive ingredients due to allergies, or need medications not commercially available. Their specializations include bioidentical hormones, peptides, weight loss formulas, and sexual wellness products, all prepared in a 503A compounding facility equipped with advanced technology and cleanroom environments.
The company operates with rigorous quality standards across every stage of production. Their laboratory maintains ISO-classified cleanrooms, uses equipment compliant with current Good Manufacturing Practice (cGMP) standards, and sources all active pharmaceutical ingredients from FDA-approved manufacturers with full traceability. Every finished product undergoes third-party testing by an independent FDA-registered laboratory for potency, sterility, endotoxin levels, pH, and particulate matter before release to patients.
CRE8 emphasizes regulatory compliance and professional oversight. They maintain non-resident pharmacy licenses throughout the United States and adhere to USP chapters 795, 797, and 800 for non-sterile compounding, sterile compounding, and hazardous drug handling respectively. The pharmacy is inspected by the Florida State Board of Pharmacy, DEA, FDA, and the Verified Pharmacy Program under the National Association of Boards of Pharmacy, with staff required to complete ongoing continuing education and procedure validation.
Longevity Contribution
- Operates a 503A compounding facility with ISO 5 and ISO 7 cleanrooms, biological safety cabinets, and state-of-the-art lyophilizer for freeze-dried powder production
- Sources all active pharmaceutical ingredients exclusively from FDA-approved manufacturers with certificates of analysis and 100% supply chain traceability
- Conducts independent third-party testing on all finished products through an FDA-registered laboratory, including potency, sterility, endotoxin, pH, and particulate analysis before release
- Holds non-resident pharmacy licenses throughout the United States and maintains compliance with USP 795, 797, and 800 standards plus DQSA requirements