Mandatory Certifications Procurement must rigorously verify supplier adherence to critical certifications, tailored to the target market and product type: For US Market Entry (Devices): Require FDA 510(k) clearance (specifically for peptide delivery), ISO 13485:2016 (Medical Devices Quality Management System), cGMP (current Good Manufacturing Practice), and ISO 9001
Important Note : The FDA doesn't approve over-the-counter skin lightening products as safe or effective
Thus, a shift toward increased clinical utility is influencing the industry competition in favor of GLP-1 receptor agonists and attracting investments into research and development projects aimed at improving therapeutic options
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