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I'm concerned that we're responding to a market-induced demand rather than a decision based in solid science, said committee member Dr
Indeed, patients are required to have measurable low antiviral Ab titers to qualify for both treatment with approved gene therapy products such as Zolgensma and for inclusion in clinical trials [358, 359]
cGMP-compliant facilities maintain documented procedures for raw materials, batch records, environmental controls, equipment validation, and traceability
These products fall outside conventional NHS prescribing practices
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