ECHA nIeuws 29-11-23

Klik op de artikels om op de hoogte te blijven van de laatste ontwikkelingen bij ECHA over volgende onderwerpen:

Intro:

ECHA identifies risks from PVC additives and microparticle releases

Reach:

European Commission decisions on applications for authorisation

• 4-(1,1,3,3-Tetra methylbutyl)phenol, ethoxylated (4-tert-OPnEO) (EC -, CAS -)
  • 1 use applied for by RSI ChemRep Europe ltd (4 January 2033)
  • 2 uses applied for by Phadia GmbH, Thermo Fisher Scientific Baltics UAB, Brahms GmbH (4 January 2033
  • 1 use applied for by Boehringer Ingelheim RCV GmbH & Co KG (19 November 2033)
• Chromium trioxide (EC 215-607-8; CAS 1333-82-0)
  • 1 use applied for by Dornbracht AG & Co. KG (31 December 2028)
  • 2 uses applied for by Ideal Standard Vidima AD and Ideal Standard Produktions-GmbH (31 December 2028)
  • 1 use applied for by Volta Energy Solutions Hungary Kft (10 January 2032)
• 4-Nonylphenol, branched and linear, ethoxylated (4-NPnEO) (EC -, CAS -)
  • 1 use applied for by Thermo Fisher Scientific Baltics UAB (4 January 2033)
• 2,2'-dichloro–4,4'-methylenedianiline (MOCA) (EC 202-918-9, CAS 101-14-4)
  • 2 uses applied for by Limburgse Urethane Castings NV (31 December 2030 and 31 December 2032)
  • 1 use applied for by 12 applicants led by Courbis Synthèse (31 August 2028)

Biocides:

• Highlights from November BPC meeting
• Support for product authorisation available
  • Post-authorisation conditions for biocidal product authorisation: harmonising practices between national and Union authorisation
  • Technical agreements for biocides entry for analytical methods and physico-chemical properties
  • Shelf-life setting during the authorisation of biocidal products
  • Post-authorisation conditions for national and simplified product authorisation: harmonising practices
• Revised procedure for managing new information on biocidal active substances
  • Management of new information on an active substance submitted for a product authorisation application
  • Overview of new active substance data submitted at product authorisation
  • Procedure for the submission, evaluation and dissemination of data generated after active substance approval
• Consultation on the draft act proposing to extend the Review Programme
• European Commission decisions on active substances

  • Commission decisions approving:

  • sulfur dioxide generated from sulfur by combustion for product-type 4; and
  • formic acid as an existing active substance for product-types 2, 3, 4 and 5.

  • Commission decision not approving:

  • silver zinc zeolite as an existing active substance for product-type 4; and
  • silver zeolite as an existing active substance for product-type 4.
• European Commission decisions on Union authorisation
  • the single biocidal product 'Hokoex'.

ECHA:

Piotr Sosnowski is new Deputy Chair of RAC

Court judgments:

Court confirms ECHA's Board of Appeal decisions on substances used in cosmetic products

Others:

REACH Committee meets in December

The next meeting of the European Commission's REACH Committee will take place on 14 December 2023. The agenda is available online.

 

 

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