diff --git a/Meeting-Highlights-from-the-Committee-for-Medicinal-Products-for-Human-Use-%28CHMP%29-12-15-December-2025.md b/Meeting-Highlights-from-the-Committee-for-Medicinal-Products-for-Human-Use-%28CHMP%29-12-15-December-2025.md new file mode 100644 index 0000000..78fe7fe --- /dev/null +++ b/Meeting-Highlights-from-the-Committee-for-Medicinal-Products-for-Human-Use-%28CHMP%29-12-15-December-2025.md @@ -0,0 +1 @@ +
The committee advisable to extend using authentic Spikevax vaccine and Spikevax bivalent Original/Omicron BA.1 as a booster dose in kids aged 6 to 11 years. The committee really helpful changing the conditional marketing authorisation of the COVID-19 vaccine Jcovden to a regular advertising authorisation. An summary of all the COVID-19 vaccines authorised in the EU is obtainable on EMA’s webpage. The agenda of the December 2022 CHMP meeting is printed on EMA's website. Minutes of the November 2022 CHMP assembly might be printed in the coming weeks. Key figures from the December 2022 CHMP meeting are represented within the graphic below. This product was designated as an orphan medication throughout its development. Orphan designations are reviewed by EMA's Committee for [Healthy Flow Blood health](https://wiki.lerepair.org/index.php/Utilisateur:JennaPitcher71) Orphan Medicinal Products (COMP) on the time of approval to determine whether or not the knowledge out there thus far allows maintaining the medicine’s orphan status and granting the medication ten years of market exclusivity.

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