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Description

doi:10.1101/2023.11.19.23298750 117

Darker lines are used for the larger subgroups

however, retatrutide has not received marketing authorisation from the Medicines and Healthcare products Regulatory Agency (MHRA) or the European Medicines Agency (EMA), and it is not approved for clinical use in the UK

It replaces traditional fax- and phone-based methods with a standardized, interoperable digital workflow embedded into electronic health record (EHR) systems and pharmacy platforms