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

(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 the technical documentation, of the minimum content of the EU declaration of conformity and of the certifi ...[+++]cates 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.

Before I get into some of the particulars of the motion, I want to ask you, Madam Speaker, to consider for a moment what it would be like to be the technician in the laboratory who has to dispose of an embryonic stem cell.

(b) in the case of second and subsequent outbreaks of avian influenza, any poultry or other birds in which clinical signs, post mortem lesions or reactions to laboratory tests carried out in laboratories approved in accordance with the first subparagraph of Article 51(3) (approved laboratory) are consistent with the diagnosis of avian influenza in accordance with the diagnostic manual;

(b) in the case of second and subsequent outbreaks of avian influenza, in which clinical signs or post mortem lesions or reactions to laboratory tests carried out in laboratories approved in accordance with the first subparagraph of Article 51(3) (approved laboratory) are consistent with the diagnosis of avian influenza in accordance with the diagnostic manual;

13. Considers it essential, in order to make for a safe, beneficial, and responsible outcome in the new biomedical research, to lay down a harmonised regulatory framework to be recognised in all parts of Europe, providing for clear-cut rules focusing not just on development, but also on scientific and technological procedures, including guidelines on good laboratory, clinical, and industrial practice geared to the latest biomedical trends; calls on the Commission to review current practices in Member States which provide for the heterogeneity of genetic testing;

I am speaking of doctors, nurses, nursing assistants, lab technicians, et cetera.