Dear Ms
<< Antragsteller:in >>,
Thank you for contacting the European Medicines Agency (EMA) to ask for information about the Vero Cell COVID-19 vaccine.
As you are aware, EMA’s human medicines committee (CHMP) started a rolling review of COVID-19 Vaccine (Vero Cell) Inactivated developed by Sinovac Life Sciences Co. Ltd. On 4 May 2021. This review remains ongoing.
During a rolling review, EMA evaluates data as they become available until EMA’s CHMP decides that sufficient evidence on the quality, safety, and efficacy of the vaccine is available. The company can then submit a formal application for marketing authorisation.
Unfortunately, we cannot comment on ongoing rolling reviews, nor can we provide an exact timeline for any rolling review as it depends on when the vaccine developer will be able to supply the required information.
EMA will communicate further when the marketing authorisation application for the vaccine has been submitted. Please refer to the following link for the latest update on COVID-19:
https://www.ema.europa.eu/en/human-regulatory/overview/public-health-threats/coronavirus-disease-covid-19/covid-19-latest-updates (
https://www.ema.europa.eu/en/human-regulatory/overview/public-health-threats/coronavirus-disease-covid-19/covid-19-latest-updates )
Please note that it is always up to individual Member States to decide whether to offer a vaccine in their vaccination programmes and to which groups. EMA is not involved in these decisions and therefore cannot advise on the future availability of a vaccine at national level, if approved.
We hope this information is of some help.
With kind regards,
Stakeholders and Communication Division
European Medicines Agency
**European Medicines Agency**
Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands
Send us a question. Go to
www.ema.europa.eu/contact ( http:://
www.ema.europa.eu/contact ) Telephone: +31 (0)88 781 6000
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We received your question(s) on: **13/05/2022**
Subject of your enquiry: **Impfung Verocell [#248925]**
Your question(s):
**Antrag nach EU-Verordnungen 1049/2001 sowie 1367/2006
Sehr geehrte Damen und Herren,
auf Basis der Verordnungen 1049/2001 sowie 1367/2006 bitte ich Sie um Übersendung von Dokumenten, die folgende Informationen enthalten:
Ich bitte um Mitteilung, wann mit einer Zulassung des chinesischen Corona-Impfstoffes Vero Cell gerechnet werden kann.
Für Ihre Bemühungen bedanken ich mich im Voraus.
Ich weise ausdrücklich darauf hin, dass ich eine Antwort per E-Mail an diese Adresse und nicht über ein Webportal wünsche. Ich möchte Sie um eine Empfangsbestätigung bitten und danke Ihnen für Ihre Mühe!
Mit freundlichen Grüßen