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If the authorisation for the “reference product” is withdrawn, can Member States also remove the relevant parallel import from the market?

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If the authorisation for the “reference product” is withdrawn, can Member States also remove the relevant parallel import from the market?

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When the authorisation for the reference product is withdrawn on grounds other than the protection of public health (for example, for reasons related to the marketing policy of the manufacturer), that should not automatically result in the withdrawal of the parallel import licence.

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