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Third-party testing for identity, potency, sterility, and endotoxin adds an extra layer of assurance

Investigators found that in many cases, high-potency, non-FDA-approved botulinum toxin products intended for research or veterinary use had been injected by unlicensed or minimally licensed providers, often in non-clinical settings

Administration Precautions: Before each administration, the vial should be inspected visually for any particulate matter or discoloration

Employing a qualitative, multi-method approach, the research integrates interviews, policy document analysis, and a review of European projects

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These suppliers have access to tens of thousands of dollars worth of equipment specifically to avoid such a scenario