Translation of "multiple choice type examination " (English → French) :

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) how 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 ...

Part one is based on multiple-choice questions to test practical and clinical knowledge, and part two is an objective/subjective clinical examination; that is, candidates are examined in 15 simulated practice situations involving standardized patients or health care professionals to test their ability to deal with common or critical practice problems.

– the applicant must pass an examination in the form of a multiple choice test;

2. For each type, the application for an EC type-examination shall be submitted by the manufacturer or his authorised representative to a notified body of his choice.

candidates completing a multiple-choice test may take the text of the questions with them when they leave the examination room unless the contents thereof are protected by copyright; the answers should also be made available to candidates;

- 2 - The approach adopted by the directive includes the following main points: - any terminal certified as conforming with the technical requirements will be authorized for marketing; - the "right of connection" to public telecommunications networks in the Community will be guaranteed for certified equipment, without the need for repeated testing and approval procedures; - the tests will be carried out and approval issued by approved laboratories and certification bodies set out in a Community list. To be on this list laboratories and bodies must meet strict criteria of competence, impartiality and independence which are harmonized at Community level; - the certificates of conformity issued under the procedure laid down by the Directive ...[+++] will be fully recognized in all Member State; - to assess conformity manufacturers will have the choice of two procedures, the EEC type-approval examination and the EEC declaration of conformity; - manufacturers will have the right to choose the laboratory or body that carries out the tests for conformity with the common technical specifications on their equipment. Accreditation of the laboratory of the manufacturer is possible as long as it satisfies the selection criteria; - the directive demands that the Member States should take all suitable measures to ensure that only terminals which meet the requirements set out in the directive are marketed. The Member States may take measures to disconnect any equipment which is not approved; - certified equipment will all bear an identical mark, namely, the "EC" mark, and other distinctive symbols making them readily identifiable.