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Partnership selection criteria reportedly emphasize: Facility Licensing and Regulatory Compliance: Current active state pharmacy licenses in good standing with no unresolved disciplinary actions Registration with state boards of pharmacy meeting all continuing requirements Registration with FDA as compounding facilities as required under federal compounding regulations Regular inspection cycles by state pharmacy board investigators or FDA when applicable Compliance history demonstrating adherence to regulatory standards Quality Control and Testing Procedures: Sourcing active pharmaceutical ingredients from FDA-registered suppliers meeting pharmaceutical-grade specifications Batch potency testing verifying semaglutide concentration matches prescribed strength Sterility testing for injectable formulations ensuring no microbial contamination Purity analysis identifying potential contaminants or degradation products Environmental monitoring in compounding clean rooms including air quality and surface contamination testing Equipment calibration and maintenance programs ensuring measurement accuracy Personnel training documentation and competency assessments Comprehensive record-keeping tracking batch numbers, production dates, and quality control results Communication and Transparency: According to platform materials, MEDVi maintains regular communication with pharmacy partners regarding: Medication quality testing reports and certificate of analysis results Product shortage situations or supply chain disruptions affecting availability Shipping delays, logistics challenges, or delivery issues requiring patient notification Patient feedback about medication effectiveness, side effects, or quality concerns Regulatory updates affecting compounding practices, formulation requirements, or distribution Understanding 503A vs

A secondary result showed that 36.8% of the group who received semaglutide had an improvement in their liver fibrosis, as well as 10.5% weight loss

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