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> Which registration does have priority: K-REACH or OSHA? Speaking about the 0.1-1 t/y registration?
> As prescribed, any person who transfers the registered substances shall provide the transferee with registration information relating to chemical substances. When shall the information be provided? How about new chemical substances that finished hazard examination under the Toxic Chemical Control Act?
> To complete substance registration under K-REACH, it is necessary to import the substance as testing sample to generate physic-chemical or hazard data. For this case, do we need to comply with K-REACH?
> Is it necessary to apply for a registration exemption when importing new chemical substances built in medical devices for in vitro diagnostic use?
> For exiting chemical substances subject to registration or new chemical substances, will they be exempt from registration if they are imported for machine test‐run purposes while are not built in the machine?
> It seems that new chemical substances should be individually registered (individual submission). Is joint submission not allowed? We think joint submission is necessary in case of repetitive generation of vertebrate test data for registration.
Company A and B are both foreign companies. Company A has obtained the registration certificate of the new chemical substance P. Company A will sell substance P to company B, and B will re-sell it to company C. Does company C need to obtain the registration certificate?
We have a product reagent in small bottles wrapped by outer boxes. How should we label it in this case?
How to determine the hazard classification of mixtures?
What chemicals need to be registered?
If the new chemical substances has already been notified under SEPA Order 17 (predecessor of MEP Order 7), is it necessary to comply with the scientific research record notification under MEP Order 7?
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