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The Medicines (Products for Human Use) (Fees) Regulations 2012
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Fee for scientific advice: application for, or variation to, EU marketing authorization
4. Unless regulation 5 applies, the fee payable by a person with whom the licensing authority holds a meeting in order to provide scientific advice with a view to that person making an application for an EU marketing authorization or an application for the variation of an EU marketing authorization, is—
(a)£2,378, if the advice provided at that meeting consists of advice in connection with—
(i)quality development only; or
(ii)safety development only;
(b)£2,986, if the advice provided at that meeting consists only of advice in connection with clinical development;
(c)£3,309, if the advice provided at that meeting consists only of advice in connection with quality and safety development;
(d)£3,917, if the advice provided at that meeting consists of advice in connection with—
(i)quality and clinical development; or
(ii)safety and clinical development;
(e)£4,849, if the advice provided at that meeting consists of advice in connection with quality, safety and clinical development.
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