European Union · Record · QUESTION_WRITTEN_PRIORITY
P-9-2022-003463
COVID-19: does authorization by the Commission lead to the liability of laboratories for compensating victims of toxic side effects?
Introduced
24 October 2022
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QUESTION_WRITTEN_PRIORITY
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Discovery layer
Source updated
24 October 2022
Records
Official record P-9-2022-003463 from European Union at European Parliament. Dated 24 October 2022. Status: QUESTION_WRITTEN_PRIORITY.
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Documents
7 official files
COVID-19: Does Commission authorisation mean that vaccine manufacturers are liable for compensating victims of toxic side effects?
COVID-19: Does Commission authorisation mean that vaccine manufacturers are liable for compensating victims of toxic side effects?
QUESTION_WRITTEN_PRIORITY · EN · 17 November 2022
COVID-19: Does Commission authorisation mean that vaccine manufacturers are liable for compensating victims of toxic side effects?
QUESTION_WRITTEN_PRIORITY · EN · 17 November 2022
COVID-19: Does Commission authorisation mean that vaccine manufacturers are liable for compensating victims of toxic side effects?
QUESTION_WRITTEN_PRIORITY · EN · 17 November 2022
Answer
QUESTION_WRITTEN_ANSWER
COVID-19: l’autorisation par la Commission entraîne-t-elle la responsabilité des laboratoires pour l’indemnisation de victimes d’effets secondaires toxiques?
QUESTION_WRITTEN_PRIORITY · FR · 17 November 2022
COVID-19: l’autorisation par la Commission entraîne-t-elle la responsabilité des laboratoires pour l’indemnisation de victimes d’effets secondaires toxiques?
QUESTION_WRITTEN_PRIORITY · FR · 17 November 2022
COVID-19: l’autorisation par la Commission entraîne-t-elle la responsabilité des laboratoires pour l’indemnisation de victimes d’effets secondaires toxiques?
QUESTION_WRITTEN_PRIORITY · FR · 17 November 2022
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