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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.
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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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23

2023.03

ECHA seeks comment on proposed PFAS restrictions

The European Chemicals Administration invites interested parties to submit scientific and technical information on the manufacture, marketing, and use of perfluorinated and polyfluoroalkyl substances (PFAS) by 25 September 2023.
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21

2023.03

ECHA identifies certain brominated flame retardants as limiting candidates

ECHA has released its flame retardant regulatory strategy, identifying aromatic brominated flame retardants as candidates for EU wide restrictions. This will minimize human and environmental exposure to these persistent.
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16

2023.03

Regulatory information | ECHA promotes SMEs to comply with authorization require

The EU-wide project of the Law Enforcement Forum on the inspection of REACH authorization responsibilities found that most users, mainly small and medium-sized enterprises, have complied with the authorization requirements to control risks.
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10

2023.03

Regulatory information | FDA proposes new rules for electronic cigarette manufac

U.S. regulators will seek the views of their advisory committees and the public on the proposed rules. The United States Food and Drug Administration is putting forward new requirements to tobacco product manufacturers on the manufacture。
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22

2023.02

REACH SVHC list may add 2 more items

On February 17, 2023, the European Chemicals Administration (ECHA) announced the public review of two SVHC candidate lists of intended substances. The review period will end on April 3, 2023.
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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

ECHA seeks comment on proposed PFAS restrictions

ECHA identifies certain brominated flame retardants as limiting candidates

Regulatory information | ECHA promotes SMEs to comply with authorization require

Regulatory information | FDA proposes new rules for electronic cigarette manufac

REACH SVHC list may add 2 more items

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