DOCUMENTS
Country
Report Expertise Centre
COUNTRY REPORT 2006 - 2007
5.3
Conformity Assessment and consumer protection
5.3.2 Conformity assessment bodies
The items below are concluded to be of most
importance remaining to be achieved
after 2006. They are not listed by priority, but marked with
the following degrees of priority:
(ST) = Short term
2007, (LT) = Long term 2008, (C) = Continuously.
5.3.1 Regulations
A list of DTM’s expectations on the development during 2007 is given
in Annex 9.
Ø
The transposition of the Council
Directive no. 2001/95 on General Product Safety (GPSD), amending
the Law no 4703 needs to be finalised (ST).
Ø
The implementation of Council
Decision 339/93 on Control of Conformity with
the Rules on Product Safety of Products
from Third Countries needs to be finalised (ST).
Ø
The prepared implementation
of EU Decision 3052/95 on Notification procedure on national
measures derogating from the free movement of goods needs
to be published (ST).
Further regulatory actions
needed:
Ø
The regulation on testing and
periodical inspection of lifts should be split up in two (LT).
Ø
The problem of products without
CE-marking transferred through EU-countries should be due
to Turkish discussions with the relevant EU country to reach
a bilateral agreement (ST).
Ø
Continued withdrawal of mandatory
standards that are hindering the free movement of goods under
implemented EU directives (C).
5.3.2 Conformity assessment bodies
Ø
UDDer and TÜRKLAB need to strengthen
their role and position in Turkish CA society (C).
Ø
TÜRKLAB should apply to the
“stakeholder members” group within EA and ILAC (LT).
Ø
TÜRKAK’s database on 1 050
public laboratories should be completed and updated with new
information and combined with the list on 1 200 conformity
assessment bodies (CABs) identified by the Ministry of Industry
and Trade as well as with the CABs identified by MEDA projects,
including the MEDA project for a TURKLAB database on CABs.
(LT+C)
Ø
Testing capacity needs to be
identified, established or extended for testing in the following
product areas: products under the LVD and Machinery directives, hot water boilers, explosives for civil use and for verification of
energy labelling (LT).
Ø
The Ministries should develop
their authorisation of test laboratories and inspection bodies
to require quality systems, assessments and preferably accreditation
as a requirement (ST).
Ø
Public laboratories have no
quality system unless they serve exporters requiring so (LT).
Ø
The Ministries should consider
privatising public test laboratories and inspection bodies.
Privatisation could promote further private investments in
sectors needing so. (LT+C).
Ø
TÜRKAK should take necessary
initiative that make EA’s internal
assessment procedures create quality and confidence in system
certification in Turkey (ST+C).
5.3.3 Notified bodies
For an efficient implementation of the EU Directives Turkey needs a
sufficient range of Notified Bodies (C).
Annex 13 presents lists of potential Turkish
NBs as identified by DTM and MIT. The lists cover total 16
CABs, besides universities, as competent to be 50 NBs to 17
directives.
Ø
An agreement between Turkey
and the EU Commission needs to be reached to make the first
three NBs operational1 and to publish further directives
to their notifications (ST).
Ø
Ministries should more actively
identify conformity assessment bodies being potential NBs. Further NB applications should be finalised
and sent to the EU Commission (ST).
Ø
It should be noted that NBs
do not need to have their own laboratories (C).
5.3.4 Safety practices
Ø
Turkey
should enforce its attempt to reach full access to RAPEX information
(ST).
Ø
Turkey
cannot prevent products without CE marking from third countries,
having a transit certificate, to enter the Turkish market
via EU member countries. The possible safety problem should
be dealt with through market surveillance activities and actions
towards the responsible importer to Turkey (C). If a problem relates to a specific country, Turkey should initiate
discussion with the relevant authorities of the member state
in order to deal with this problem. (ST+C).
Ø
Further awareness campaigns
are needed to improve both manufacturers’ and consumers’ knowledge
on CE-marking, the necessity of CE-marking also within Turkey
and also to eliminate the misunderstanding of CE-marking being
a quality mark (C).
Ø
To eliminate the risk of unfair
competition and to avoid the sales of unsafe products Turkey
should ensure, through market surveillance, that all
Ø
manufacturers properly apply
CE-marking (C).
Ø
Market surveillance activities
must include the Internet market as part of the totalmarket
(C).
Ø
The Government should activate
consumers’ organisations by offering them financial support
(C).
Ø
The Market Surveillance Coordination
Board is recommended to have a decision-making role and the
market surveillance authorities should
continue to organize seminars for the civil society (C).
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