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Autoridad Nacional Competente
(CNA)
published: 07 ene. 2010
last updated: 21 ene. 2021
European Food Safety Authority (EFSA) GMO Panel
Via Carlo Magno 1A
Parma,
43126,
Italia
- +39 0521 036 666
- European Food Safety Authority (EFSA) [ English ]
Persona:Dr. Ana AfonsoHead of Unit, GMO UnitVia Carlo Magno 1AParma, PR
43126, ItaliaTeléfono: +39 0521 036 666,Fax:Correo electrónico: GMO_secretariat_applications@efsa.europa.eu, international.cooperation@efsa.europa.eu,Sitio web: https://www.efsa.europa.eu/,Organización relacionadaEuropean Food Safety Authority (EFSA)Organismo gubernamental (nacional/federal)Via Carlo Magno 1AParma, PR
43126, ItaliaTeléfono: +39 0521 036 666,Fax:Correo electrónico: GMO_secretariat_applications@efsa.europa.eu, international.cooperation@efsa.europa.eu,Sitio web: https://www.efsa.europa.eu/,
No
The EFSA GMO Panel provides independent scientific advice on the safety of genetically modified organisms (GMOs).
The Panel carries out risk assessments in order to produce scientific opinions and advice for risk managers. Its risk assessment work is based on reviewing scientific information and data in order to evaluate the safety of a given GMO. This helps to provide a sound foundation for European policies and legislation and supports risk managers in taking effective and timely decisions. The Panel carries out much of its work in the context of authorisation applications, since all GM food and feed products must be evaluated by EFSA before they can be authorised in the EU.
The Panel carries out risk assessments in order to produce scientific opinions and advice for risk managers. Its risk assessment work is based on reviewing scientific information and data in order to evaluate the safety of a given GMO. This helps to provide a sound foundation for European policies and legislation and supports risk managers in taking effective and timely decisions. The Panel carries out much of its work in the context of authorisation applications, since all GM food and feed products must be evaluated by EFSA before they can be authorised in the EU.
| Tipo de registro | Campo | Registro(s) | |
|---|---|---|---|
| Evaluación del riesgo generada por un proceso regulatorio | Autoridad(es) Nacional(es) Competente(s) responsable(s) por la evaluación del riesgo | 191 | |
| Leyes, reglamentos, directrices y acuerdos en materia de seguridad de la biotecnología | Autoridad(es) nacional(es) competente(s) y/o Autoridad(es) competente(s) en el Protocolo suplementario | 10 | |
