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2010 ilerleme raporu - Avrupa Birliği Bakanlığı

2010 ilerleme raporu - Avrupa Birliği Bakanlığı

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methods for such instruments, the international system for units of measurement and nominal<br />

quantities of pre-packed products. Although progress has been made towards further<br />

alignment, full implementation of the Measuring Instruments Directive has not yet been<br />

achieved.<br />

There was some progress on market surveillance. The Under-Secretariat of Foreign Trade<br />

issued legislation to lay down a common template for market surveillance reports and<br />

notifications. A national surveillance strategy for <strong>2010</strong>-2012 has been adopted. The Ministry<br />

of Industry and Trade and the Ministry of Agriculture published legislation for organisational<br />

aspects of market surveillance activities. The Under-Secretariat’s report on market<br />

surveillance activities in 2009 is a major step towards systematic collection of comparable<br />

surveillance data, even though a number of authorities were unable to contribute basic data.<br />

Market surveillance activities have continued to increase, even though some product<br />

categories deserve more focus, such as civil explosives, detergents, machinery and the nonharmonised<br />

area in general. Financial and human resources devoted to market surveillance are<br />

insufficient; in particular, more full-time specialised inspectors are needed. The use of<br />

appropriate risk assessment and sampling methods, which would help optimise the use of<br />

limited market surveillance budgets, remains limited, as is the evaluation of the effectiveness<br />

of the action taken. There is no database linking accidents and injuries to products. The<br />

visibility of market surveillance remains low. Coordination within and between surveillance<br />

agencies is still deficient, including on use of IT. Stakeholders are not systematically informed<br />

of market surveillance activities and measures and their general involvement in surveillance<br />

remains weak. In particular, consumer organisations need to be supported in order for them to<br />

better understand technical legislation and to use complaint mechanisms more effectively.<br />

Full alignment with the 2001 version of the general products safety directive remains<br />

outstanding. Full and systematic implementation of Regulation 765/2008, setting out the<br />

requirements for accreditation and market surveillance relating to the marketing of products,<br />

remains to be ensured, including provisions on external border controls.<br />

Alignment of horizontal measures is advanced. However, effective implementation of market<br />

surveillance and adoption of final changes to the legislation on standardisation and<br />

accreditation have yet to be achieved. Furthermore, the new legislative framework on<br />

marketing of products has yet to be adopted in the areas of market surveillance, conformity<br />

assessment procedures, CE marking and accreditation.<br />

Further progress was made on the old approach acquis. The Ministry of Industry and Trade<br />

adopted various pieces of legislation on the type approval of motor vehicles and emissions<br />

from vehicles and tractors. In particular, the Ministry of Trade and Industry published a<br />

regulation concerning the type approval of motor vehicles with regard to their reusability,<br />

recyclability and recoverability aiming to transpose the related EC Directive on the same<br />

subject. The same Ministry published a regulation and an implementing communiqué aiming<br />

to transpose the EC Regulation on the type approval of motor vehicles with regard to the<br />

protection of pedestrians and other vulnerable road users. The Ministry of Health issued an<br />

amending regulation regarding the packaging and labelling of pharmaceutical products for<br />

human use. The same Ministry issued an amending regulation on the pricing of<br />

pharmaceuticals for human use and provisions were adopted on clinical trials. The problem of<br />

protection of regulatory data persists and the authorisation system for generic medicines for<br />

which marketing authorisation was applied prior to 1 January 2005 remains in place. Turkey<br />

is continuing to violate the Customs Union obligations in this area. The Ministry of the<br />

Environment and Forestry issued a regulation on good laboratory practice which is of key<br />

importance for the chemicals sector. The requirements imposed on imports of alcoholic<br />

EN 46 EN

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