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However, the MHRA's regulatory framework for unlicensed medicines known as 'Specials' is directly relevant
What plaintiffs must demonstrate is that the drug is capable of causing the alleged harm, that their injury is consistent with known risks, and that the manufacturer failed to warn them appropriately
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a Purported location listed on website
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GLP-1s offer a promising new tool in addressing this challenge, which is why physicians, patients, and policymakers are all paying close attention
