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Patient & Consumer Protection / Pharmaceutical care | Webinar | 16 June 2021 | Strasbourg, France
Before administration to patients, parenteral medicines must be in a ready-to-administer (RTA) form, presented at the required concentration and volume, in the final container (syringe, infusion bag or elastomeric device) for administration. Unless provided by the marketing authorisation holder in an RTA form, parenteral medicines have to be reconstituted.