Traduction de «inspector » (Anglais → Français) :

...down by province, of (i) inspectors at the CFIA, (ii) newly hired inspectors at the CFIA, (iii) inspectors who retired from the CFIA, (iv) employees assigned to the CFIA Process, Formulation and Label Registration Unit; (b) what is the total number, for each of the fiscal years from 2005-2006 to 2011-2012, across Canada as a whole and broken down by province, of inspections conducted by a CFIA inspector of a product at a dealer, broken down by (i) retailer, (ii) manufacturer, (iii) processor, (iv) producer, (v) business engaged in importing any product, (vi) business engaged in packing any product, (vii) business engaged in selling a ...[+++]ny product; (c) for the answer to each part of (b), was the inspection at (i) a site randomly selected, (ii) a site in which the inspection was pre-arranged with any of the individuals or groups identified in (b); (d) for the answer to each part of (c), was the reason for the inspection related to (i) misleading advertising or labelling of exaggerated or unproven nutrition and health claims, (ii) misleading labelling information of the country of origin claims; (e) for the answer to each part of (b), (c) and (d), how many, (i) products or any labelling, packaging or advertising materials were seized and detained by the inspectors, (ii) cases of non-compliance were identified during inspections; (f) for the answer to each part of (e), how many inspections lead to (i) the prosecution of an individual, (ii) the prosecution of a dealer, (iii) a summary conviction or a conviction on indictments of an individual with a fine, (iv) a summary conviction or a conviction on indictments of a dealer with a fine, (v) a summary conviction or a conviction on indictments of an individual with a prison term? ...

Question No. 310 Mr. Malcolm Allen: With respect to the Canadian Food Inspection Agency’s (CFIA) animal transportation inspection system and review of the animal transport regulations under the Part XII of the Health of Animals Regulations: (a) how many full-time CFIA inspectors are stationed across the country to inspect animal welfare and ensure compliance with Part XII of the Health of Animals Regulations; (b) what positions and titles do these inspectors hold; (c) how many of these inspectors hold the title or position of animal health inspector; (d) how many of these inspectors hold the title or position of multi-program inspecto ...[+++]r; and (e) do draft amendments or proposals to the animal transport regulations under the Health of Animals Regulations, Part XII, exist and, if so, what is the Agency’s timeframe for publishing those proposed changes in Part I of the Canada Gazette?

3. Inspection and surveillance reports drawn up by Commission inspectors, Community inspectors, inspectors of Member States or inspectors of a third country, which is party to the agreement concerned, shall constitute admissible evidence in administrative or judicial proceedings of any Member State.

2. Where, in accordance with Article 122 of Directive 2001/83/EC, the Commission is informed of serious differences of opinion between Member States as to whether the holder of the marketing authorisation for the medicinal product for human use or a manufacturer or importer established within the Community satisfies the requirements referred to in paragraph 1, the Commission may, after consultation with the Member States concerned, request an inspector from the supervisory authority to undertake a new inspection of the marketing authorisation holder, the manufacturer or the importer; the inspector in question shall be accompanied by two ...[+++] inspectors from Member States which are not party to the dispute or by two experts nominated by the Committee for Medicinal Products for Human Use.

2. Where, in accordance with Article 90 of Directive 2001/82/EC, the Commission is informed of serious differences of opinion between Member States as to whether the holder of the marketing authorisation for the veterinary medicinal product or a manufacturer or importer established within the Community satisfies the requirements referred to in paragraph 1, the Commission may, after consultation with the Member States concerned, request an inspector from the supervisory authority to undertake a new inspection of the holder of the marketing authorisation, the manufacturer or the importer; the inspector in question shall be accompanied by ...[+++]two inspectors from Member States which are not party to the dispute and/or by two experts nominated by the Committee for Medicinal Products for Veterinary Use.

This might involve finding out what the Member States are doing in terms of inspections, consultation and training, with a view to sharing best practice, involving the Senior Labour Inspectors Committee (SLIC),[34] and encouraging national labour inspectorates to focus on the sector and to consider forms of cooperation with other inspectorates, in particular technical and health inspectorates, where applicable.