Traduction de «Technicienne de laboratoire médical » (Français → Anglais) :

medical laboratory technologist | laboratory technologist | medical technologist | medical laboratory technician | medical laboratory assistant

laboratory technician, asphalt | technical supervisor, asphalt production | asphalt laboratory technician | asphalt production technical supervisor

leather dye and chemical coordinator | leather testers | leather chemical technician | leather laboratory technician

footwear quality control engineer | footwear quality control laboratory technologist | footwear quality control laboratory analyst | footwear quality control laboratory technician

combined laboratory and x-ray technician

medical laboratory technician

Medical Laboratory Technician [ ML TC ]

laboratory technician

Medical Laboratory Technician

animal care technician | laboratory animal technician

P. whereas the Ebola epidemic has highlighted serious shortcomings in local health crisis prevention; whereas the international community’s response to the countries affected by Ebola should include different elements, such as laboratory capacity to diagnose and confirm infection, awareness-raising, improving the commitment of the community and cultural comprehension, social mobilisation, contact tracing and monitoring, alerts and surveillance, access to health care for non-Ebola patients and ensuring safe funerals; whereas the protection of both health facilities, which are still lacking in parts of West Africa, and health workers, wh ...[+++]o play a key role in such emergency circumstances, should be developed through an emergency medical training programme to overcome the acute shortage of local medical staff and to contain the epidemic;

(64) In order to maintain a high level of health and safety, the power to adopt acts in accordance with Article 290 TFEU should be delegated to the Commission in respect of the products subject to this Regulation that are similar to medical devices but do not necessarily have a medical purpose; adaptation of the definition of nanomaterial to technical progress and to developments at Union and international level; adaptation to technical progress of the general safety and performance requirements, of the elements to be addressed in t ...[+++]he technical documentation, of the minimum content of the EU declaration of conformity and of the certificates issued by notified bodies, of the requirements to be met by notified bodies, of the classification rules, of the conformity assessment procedures, and of the documentation to be submitted for the approval of clinical investigations; the establishment of the UDI system the information to be submitted for the registration of medical devices and certain economic operators; the level and structure of fees for the designation and monitoring of notified bodies; the publicly available information in respect of clinical investigations; the adoption of preventive health protection measures at EU level; and the tasks of and criteria for European Union reference laboratories and the level and structure of fees for scientific opinions delivered by them.

(64) In order to maintain a high level of health and safety, the power to adopt acts in accordance with Article 290 TFEU should be delegated to the Commission in respect of the products subject to this Regulation that are similar to medical devices but do not necessarily have a medical purpose; adaptation of the definition of nanomaterial to technical progress and to developments at Union and international level; adaptation to technical progress of the general safety and performance requirements, of the elements to be addressed in t ...[+++]he technical documentation, of the minimum content of the EU declaration of conformity and of the certificates issued by notified bodies, of the minimum requirements to be met by notified bodies, of the classification rules, of the conformity assessment procedures, and of the documentation to be submitted for the approval of clinical investigations; the establishment of the UDI system; the information to be submitted for the registration of medical devices and certain economic operators; the level and structure of fees for the designation and monitoring of notified bodies; the publicly available information in respect of clinical investigations; the adoption of preventive health protection measures at EU level; and the tasks of and criteria for European Union reference laboratories and the level and structure of fees for scientific opinions delivered by them.

45. Stresses the importance of research in the medical sector, which, combined with innovative applications, will foster growth and well-being in an ageing society; supports close co-operation between university research departments and the medical industry in order to generate products and services that citizens in the EU will urgently need over the next decade;