Statute-Shenzhen DTi Technology Testing Co., Ltd.

05

2023.05

EU ECHA provides recommendations on new hazard categories for substances and mix

The three new hazard categories for classification, labeling, and packaging (CLP) substances and mixtures will take effect on April 20, 2023. ECHA has released information on application dates and related guidelines.
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05

2023.05

EU ECHA: Reliable Research Summary Effectively Supports Hazard Assessment

The final report of the OECD project led by ECHA on the role of robust research abstracts in chemical hazard assessment was found to be in line with the objectives.
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04

2023.05

France considers banning disposable e-cigarette products

The ban may become part of a new anti smoking plan being developed by the Ministry of Health over the next five years.
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04

2023.05

Regulatory Information | Australia Will Ban All Imports of Over the Counter Elec

The Australian government announced on May 1st that it will ban the import of all over-the-counter e-cigarette products, including those that do not contain nicotine.
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23

2023.04

EU 2023 New Hazard Level Declaration

The European Commission has issued an authorized regulation to amend the CLP regulation, which stipulates new hazard categories and standards for the classification, labeling, and packaging of substances and mixtures.
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23

2023.04

ECHA provides recommendations on new hazard categories for substances and mixtur

The three new hazard categories for classification, labeling, and packaging (CLP) substances and mixtures will take effect on April 20, 2023. ECHA has released information on application dates and related guidelines.
View details
23

2023.04

What are the European Union Classification, Labelling and Packaging Regulations?

The EU Classification, Labeling, and Packaging (CLP) regulation (EC) No 1272/2008) requires manufacturers, importers, or downstream users of substances or mixtures to properly classify, label.
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17

2023.04

Pre Sales Tobacco Product Application (PMTA) in the United States

According to section 910 (b) of the Federal Food, Drug, and Cosmetic (FD&C) Act, anyone can submit a Pre Market Tobacco Product Application (PMTA) for any new tobacco product seeking FDA marketing orders.
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17

2023.04

Regulatory Information | New Resources to Assist in Submitting PMTA Amendments

The Tobacco Products Center (CTP) of the US Food and Drug Administration has created two new resources to assist applicants in preparing and submitting amendments to their pre market tobacco product application (PMTA):
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13

2023.04

ECHA recommends eight substances for REACH authorisation

To protect workers and the environment, ECHA recommends that the European Commission add eight substances, including lead, to the REACH authorization list. Once substances are added to the list。
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EU ECHA provides recommendations on new hazard categories for substances and mix

EU ECHA: Reliable Research Summary Effectively Supports Hazard Assessment

France considers banning disposable e-cigarette products

Regulatory Information | Australia Will Ban All Imports of Over the Counter Elec

EU 2023 New Hazard Level Declaration

ECHA provides recommendations on new hazard categories for substances and mixtur

What are the European Union Classification, Labelling and Packaging Regulations?

Pre Sales Tobacco Product Application (PMTA) in the United States

Regulatory Information | New Resources to Assist in Submitting PMTA Amendments

ECHA recommends eight substances for REACH authorisation

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