Traduction de «Valve body » (Anglais → Français) :

valve body flange

throttle valve body assembly [ throttle valve housing ]

needle-valve housing | valve body

lug-wafer butterfly valve | lug wafer butterfly valve | lug body valve | lug-type butterfly valve | lug-type valve | single-flanged valve

cover | dome | valve body

throttle body | TB | throttle valve body | throttle housing | throttle-valve housing | fuel charging station

EU office or agency [ autonomous Community body | Community service body | decentralised Community body | EC institutional body | EC satellite body | EC specialised body | EU Agencies and decentralised bodies | European agency | European foundation | European Monitoring Centre | European Union office or agency | specialised Community agency ]

valve-spring compressor | valve spring compressor | valve spring lifter | valve-spring lifter | valve spring tool | valve spring compressor tool | valve-spring compressor tool

public institution [ body under public law | NDPB | non-departmental public body | public body | Quango | quasi-autonomous non-governmental organisation | quasi-autonomous non-governmental organization | Public law institutions(ECLAS) ]

EU body [ Community body (established by the Treaties) | European Union body ]

Question No. 53 Ms. Kirsty Duncan: With respect to the chronic cerebrospinal venous insufficiency (CCSVI) clinical trial being undertaken by Dr. Traboulse: (a) what milestones are reportable to the government, (i) on what date(s) is reporting expected to occur, (ii) how will this information be communicated to patients, the medical community, and the general public; (b) on what date did each of the trial sites pass ethical review; (c) on what date did recruitment of patients begin for each of the trial sites; (d) how many patients with multiple sclerosis (MS) are being recruited for each site, and how is consistency in diagnosis and treatment being ensured across sites; (e) who is performing the diagnoses for CCSVI for each site, (i) ho ...[+++]w is the diagnosis being performed, including, but not limited to, ultrasound and venogram, (ii) how many diagnoses has each person undertaking the diagnosis at each site performed prior to the study, and by whom was each person trained; (f) who is performing the procedures for each site, (i) how is the procedure being performed, including, but not limited to, anesthetic, balloon size, (ii) how many procedures has each person undertaking the procedure at each site performed prior to the study, and by whom was each person trained; (g) what are the selection criteria for the trial, including, but not limited to, type of MS, Expanded Disability Status Scale (EDSS) score, venous abnormality/malformed valve/stenosis, mobility, (i) how do these criteria compare with the international literature, (ii) with how many international studies to date will the selection criteria be analytically comparable; (h) if both progressive and relapsing-remitting forms of MS are to be examined in the trial, how will statistical significance be ensured given that 50 of 100 patients will undergo a “sham” procedure, 25 patients will have a progressive form of the disease, and 25 will have a relapsing-remitting form of the disease, and will people with bo ...

5a. Where pressure receptacles were manufactured in a series, Member States may authorise the reassessment of conformity of individual pressure receptacles, including their valves and other accessories used for transport, to be carried out by a notified body notified for periodic inspection of the relevant transportable pressure receptacles provided that conformity of the type has been assessed in accordance with paragraph 3 by a type A notified body, responsible for reassessment of conformity, and a certificate of type reassessment i ...[+++]ssued.

4. Where pressure receptacles were manufactured in series, Member States may authorise the assessment of conformity of individual pressure receptacles, including their valves and other accessories used for transport, to be carried out by a notified body conforming to EN ISO/IEC 17020:2004 Type B provided that conformity of the type has been assessed in accordance with paragraph 3 by a type A notified body.

5. Where pressure receptacles were manufactured in series, Member States may authorise the reassessment of conformity of individual pressure receptacles, including their valves and other accessories used for transport, to be carried out by a notified body notified for periodic inspection of the relevant transportable pressure receptacles provided that conformity of the type has been assessed in accordance with paragraph 3 by a type A notified body, responsible for the reassessment of conformity, and a certificate of type reassessment ...[+++]issued.