82It follows from all the foregoing considerations that the scope of a global marketing authorisation, as defined in the second subparagraph of Article 6(1) of Directive 2001/83, as amended, encompasses developments for which separate marketing authorisations have been granted under the centralised procedure. The fact that Novartis was able to obtain, by means of that procedure, a marketing authorisation for new therapeutic indications with a new name, namely Aclasta, is therefore irrelevant for the purpose of the application of the regulatory data protection period.
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