Tradução de«diretora de laboratório médico » (Português → Inglês) :

medical laboratory administrator | medical laboratory supervisor | clinical laboratory supervisor | medical laboratory manager

chief science officer | head laboratory analyst | research manager | reserach managers

clinical laboratory

keep medical laboratory equipment in appropriate condition | maintain equipment of medical laboratories | check medical laboratory equipment | maintain medical laboratory equipment

Agreement on the Temporary Importation, free of duty, of Medical, Surgical and Laboratory Equipment for use on free loan in Hospitals and other Medical Institutions for purposes of Diagnosis or Treatment

Laboratory medicine — Requirements for reference measurement laboratories (ISO 15195:2003)

To raise Nation-wide awareness of internationally agreed normative documents of relevance, namely the European Committee for Standardization (CEN) Workshop Agreement, ISO 15793:2011 Laboratory biorisk management, ISO 15189:2007 Medical laboratories — Particular requirements for quality and competence, ISO 15190:2003 Medical laboratories — Requirements for safety, ISO/IEC 17025:2005 General requirements for the competence of testing and calibration laboratories, ISO 9001:2008 Quality management systems — Requirements, as well as ISO 14001:2004 Environmental management systems — Requirements with guidance for use, involving national health ...[+++] policy makers as well as laboratory managers and staff who are encouraged to commit to a transparent and accountable culture of biosafety, biosecurity and laboratory quality systems.

To raise Nation-wide awareness of internationally agreed normative documents of relevance, namely the European Committee for Standardization (CEN) Workshop Agreement, ISO 15793:2011 Laboratory biorisk management, ISO 15189:2007 Medical laboratories — Particular requirements for quality and competence, ISO 15190:2003 Medical laboratories — Requirements for safety, ISO/IEC 17025:2005 General requirements for the competence of testing and calibration laboratories, ISO 9001:2008 Quality management systems — Requirements, as well as ISO 14001:2004 Environmental management systems — Requirements with guidance for use, involving national health ...[+++] policy makers as well as laboratory managers and staff who are encouraged to commit to a transparent and accountable culture of biosafety, biosecurity and laboratory quality systems.

(iii) proven laboratory experience in one of the following areas: testing or calibration laboratory, supervisory authority or institution, national reference laboratory for class D devices, quality control of in-vitro diagnostic medical devices, development of reference materials for IVDs, calibration of diagnostic medical devices; laboratories or blood banks which experimentally assess and use high-risk IVDs or, where applicable, manufacture them in-house;

proven laboratory experience in one of the following areas: testing or calibration laboratory, supervisory authority or institution, national reference laboratory for class D devices, quality control of in-vitro diagnostic medical devices, development of reference materials for IVDs, calibration of diagnostic medical devices; laboratories or blood banks which experimentally assess and use high-risk IVDs or, where applicable, manufacture them in-house.

(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 certificates issued by notified bodies, of the minimum requirements to be met by notified bodies, of the classific ...[+++]ation 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 the 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 ru ...[+++]les, 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.

Cooperation between Member States, Medical Device Coordination Group, Medical Device Advisory Committee, EU reference laboratories, device registers

Cooperation between Member States, Medical Device Coordination Group, Medical Device Advisory Committee, EU reference laboratories, device registers

Cooperation between Member States, Medical Device Coordination Group, EU reference laboratories, device registers

A common set of five different tyres, conforming to the specification of section 2.2 shall be measured in accordance with section 2.3 by the candidate laboratory and by one reference laboratory.

2. The expanded uncertainties (k = 2) of the mean of the repeated measurements in laboratory 1 and of the mean of the repeated measurements in laboratory 2 are

The European Commission has decided to refer France, Germany, Italy and Portugal to the Court of Justice for restrictions on the services of medical laboratories, patent agents, engineers and private security firms respectively, which it considers violate EC Treaty rules on the freedom to provide services (Article 49) and the freedom of establishment (Article 43).

French legislation (Decree N° 76-1004) does not allow a medical laboratory established in another Member State to undertake medical analyses in France unless it has a licensed operating establishment on French territory.

The Commission has also sent formal requests to Austria, France, Greece and Portugal to put an end to restrictions affecting respectively patent agents, medical laboratories, opticians shops and private security services.

These devices are used mainly by medical laboratories, doctors and pathologists.

The objective is to support projects to develop the calibration means required by testing laboratories in the Community, to ensure that measurements and tests are done on a common basis and can be compared also with measurements done outside the Community.

With regard to physical measurements, transfer standards will be developed to enable smaller national metrology laboratories to establish relations and traceability of measurements with larger organizations. This will be done with particular attention to the needs of the newer Member States.

Whereas, apart from the benefit to patients, it is also recognized that improved training for the specific function of general medical practitioner would contribute to an improvement in health care, particularly by developing a more selective approach to the consultation of specialists, use of laboratories and other highly specialized establishments and equipment;

This exclusion is absolutely unacceptable in the Committee's view; it believes that the directive should cover all control materials, irrespective of whether or not they are used in medical laboratories.