Individual Registration

REACH Integra pays special attention to two different aspects when it comes to participating in a Joint Submission and preparing an Individual Registration Dossier. On one hand, the similarity of substances is taken into consideration. Previous characterisation analysis will determine the suitability as to participation in a Joint Submission for that particular substance.

On the other hand, the uses and the Chemical Safety Report included in the Registration Dossier as well as the suitability for classification and labelling are the main aspects taken into consideration in determining whether participation in a Joint Registration would fulfil all the reporting requirements.

REACH Integra performs all the necessary tasks to prepare the Registration Dossier and to register substances:

• Late Pre-registration of Phase-in Substances
• Preparation and Submitting of the Inquiry Dossier to ECHA for Phase out Substances
• Preparation and Submitting of the Individual Registration Dossier to ECHA:
  • General Individual Registration
  • Individual Registration of In situ Isolated Intermediates
  • Individual Registration of Transported Isolated Intermediates

Identification of Substances

The analytical identification of substances is of great importance in substance registration and, particularly, in the Inquiry Dossier of phase out substances.

REACH Integra does not carry out the analytical characterisation studies for substances; however, through the following services REACH Integra analyzes identification alternatives for the substance to be registered and the analytical capabilities of the client company:

• Advice on the structural characterisation and determination of the quantitative composition, characterisation testing proposal
• Laboratory management processes, outsourcing and monitoring of characterization studies: IR, NMR, HPLC, GC, UV, XRD, XRF, ICP, elemental analysis, DSC, etc.

In order to give support for registration, all REACH Integra services are complemented by consulting and representation services in the SIEF and Consortia, for the purpose of gathering all necessary information, acquiring Letters of Access and classification and labelling notifications for substances and participating in the Joint Submission, etc.