F.A.Q

1

What is Biocidal Product?

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What Regulations are Followed in the Biocidal Product Registration Process?

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2

3

What should be done for products falling within the scope of the Biocidal Product Regulation?

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What is the criteria for a Non-Medical Veterinary Health Product to be Placed on the Turkish Market?

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What are our Compliance Services for the Regulation on Non-Medical Veterinary Health Product?

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14

15

Is the Turkish SDS must be prepare according to which regulation? What is the purpose of this Regulation?

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What is Safety Data Sheet (SDS) and which on conditions is it prepared?

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16

17

What are the out of scope for Safety Data Sheet?

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Who can prepare Turkish SDS?

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18

19

What are the elements that need to be in Turkish labels?

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What is Turkish KKDIK?

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20

21

What is the meaning of KKDIK?

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Are there any separation of deadlines for KKDIK Registration?

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22

23

How will the companies which are exporting chemicals to Turkey act regarding KKDIK registration?

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Are there any lowest volume threshold regarding the C&L notification obligation?

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24

25

Shall the imported non-hazardous substances (either on their own or in a mixture) be notified to the C&L inventory?

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Which substances will be notified to Turkish C&L inventory?

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26

27

Will the ELINCS listed substances be notified to the Turkish C&L inventory?

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How the notifications to C&L inventory be submitted?

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28

29

What are the other conditions that the SEA Regulation shall not apply to?

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What are the responsibilities of manufacturers and importers of chemicals in the scope of Turkish CLP Regulation?

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30

31

Who can submit a C&L notification?

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Does any official fees apply for the C&L notifications?

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32

33

Which substances and mixtures are in the Scope of the New Turkish CLP Regulation?

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What is the purpose of the New Turkish CLP Regulation?

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34

35

What are the main differences of Turkish CLP from CPL Regulation?

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For which type of products the C&L Notification obligation and other obligations of the SEA regulation does not apply?

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36

37

What are the general labelling principles of Turkish CLP Regulation and what are the information to be mentioned on the labels of substances & mixtures?

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EU CLP Application Date?

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38

39

Which substances do I have to notify to the Inventory?

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What is Notification under the CLP Regulation?

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40

41

Which Turkish governmental departments are responsible for these regulations?

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In brief, what has changed regarding the chemical regulations in Turkey?

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42

43

What are the duties of suppliers and the importers for a continuous benefit from notifications?

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Will the importer information be kept confidential ?

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44

45

Which type of data are required about the importer ?

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Why is the importer data needed ?

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46

47

Is there any potential extension of the deadline ?

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What has been changed with the new IT system ?

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48

49

When was the new ITversion released and when did it become functional ?

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Why a new release is required by MoEF ?

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50

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F.A.Q

SEARCH

What is Biocidal Product?

What Regulations are Followed in the Biocidal Product Registration Process?

What should be done for products falling within the scope of the Biocidal Product Regulation?

What are our services within the scope of the Biocidal Products Regulation?

How long does the Biocidal Product Licensing Process take?

In which Laboratory are Biocidal Product Analyzes Performed?

Treated Articles or Biocidal Products?

Is Active Substance Registration done in Turkey?

What is the Ingredient Data Sheet for Detergents Regulation?

How The Packages Should Be Labelled Which Is Not Exceeding 125 Ml?

Is The Certificate Expire Safety Data Sheets (SDS) Should Be Updated?

What is the Non-Medical Veterinary Health Product?

What is the criteria for a Non-Medical Veterinary Health Product to be Placed on the Turkish Market?

What are our Compliance Services for the Regulation on Non-Medical Veterinary Health Product?

Is the Turkish SDS must be prepare according to which regulation? What is the purpose of this Regulation?

What is Safety Data Sheet (SDS) and which on conditions is it prepared?

What are the out of scope for Safety Data Sheet?

Who can prepare Turkish SDS?

What are the elements that need to be in Turkish labels?

What is Turkish KKDIK?

What is the meaning of KKDIK?

Are there any separation of deadlines for KKDIK Registration?

How will the companies which are exporting chemicals to Turkey act regarding KKDIK registration?

Are there any lowest volume threshold regarding the C&L notification obligation?

Shall the imported non-hazardous substances (either on their own or in a mixture) be notified to the C&L inventory?

Which substances will be notified to Turkish C&L inventory?

Will the ELINCS listed substances be notified to the Turkish C&L inventory?

How the notifications to C&L inventory be submitted?

What are the other conditions that the SEA Regulation shall not apply to?

What are the responsibilities of manufacturers and importers of chemicals in the scope of Turkish CLP Regulation?

Who can submit a C&L notification?

Does any official fees apply for the C&L notifications?

Which substances and mixtures are in the Scope of the New Turkish CLP Regulation?

What is the purpose of the New Turkish CLP Regulation?

What are the main differences of Turkish CLP from CPL Regulation?

For which type of products the C&L Notification obligation and other obligations of the SEA regulation does not apply?

What are the general labelling principles of Turkish CLP Regulation and what are the information to be mentioned on the labels of substances & mixtures?

EU CLP Application Date?

Which substances do I have to notify to the Inventory?

What is Notification under the CLP Regulation?

Which Turkish governmental departments are responsible for these regulations?

In brief, what has changed regarding the chemical regulations in Turkey?

What are the duties of suppliers and the importers for a continuous benefit from notifications?

Will the importer information be kept confidential ?

Which type of data are required about the importer ?

Why is the importer data needed ?

Is there any potential extension of the deadline ?