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7. For procedural or regulatory queries related to Type I variations for medicines for human use, MAHs can send an email to: [email protected]ema. This applies to all new and existing applications and all types of submissions to the European Medicines Agency (EMA). .
Types of Aggregate reports. Submitting a post-authorisation application. Preparing your work for electronic submission 4.
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435d71049abcc88e2a7e. This submission type is the most widely used by MAHs to report the current marketing status of medicinal products currently markted in the EU/EEA MS.
