Contacts

Helsinki
HTC Keilaniemi
Keilaranta 15
FI-02150 Espoo

Tel. +358(0) 9 412 3055
Fax: +358 (0) 9 412 3049


Brussels
Avenue Franklin Roosevelt 135/23
B-1050 Brussels
Belgium

Tel. +358(0) 9 412 3055
Fax: +358 (0) 9 412 3049


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Registration services

Late Preregistration 

We prepare and submit a late pre-registration on behalf of you. Also, the downstream users will be notified of a successful pre-registration and you will receive the submission report of the pre-registration of your substance.  Late pre-registration is possible under the following conditions:

  1. The substance was not facture or imported to the EU between 1.6.2008 – 1.12.-2008 in quantities above 1 tone/year.
  2. The pre-registration will take place after 1st of December 2008, within six months of first manufacturing importing or using the substance in quantities of one tone or more per year and no later than 12 months before the relevant deadline in Art. 23.

 

REACH Registration

We act for our customers in the REACH Registration process as a representativeof the lead registrant, as only representative or third party representative depending on the customer´s need. With our multidisciplinary team of experts we take our customers through the different phases of the registration process Pre-SIEF, SIEF and Consortium.

Also, we provide resources and expertise for the hazard assessment, exposure assessment and risk characterization when needed.  We provide the Customer with a complete Chemical Safety Report and if collection of information in supply chain is required, we provide resources and expertise to perform the work, as such as complete technical dossier in IUCLID5 format and submit the dossier to ECHA using REACH-IT.

Finally we provide resources and expertise for the classification and labelling of the substances for their physical, health and environmental hazards. Classification and labelling will be done according to new GHS-system.


Intermediate substances

If your company manufacturer intermediate substances we provide you the following services, case by case, to be compliant with REACH:

Potential Fast Lane Registration of Intermediate manufacturer
Determination of “strictly controlled conditions” – status
Preparation of the intermediate registration dossier with associated testing.
 

Lead Registrant

The lead registrant takes on the legal responsibility under Article 11 of REACH for executing joint submission in time so that other registrants can follow suit in due course. The Cefic recommended deadline for the joint submission of high volume, CMR 1 and 2 and R 50 and 53 substances is 1st June 2010. Yet, currently less than 10% of pre-registered substances have a Lead Registrant.

Some lead registrants can rely on the support of a consortium, industry association or a research institute. Others have been alone in initiating pre-SIEF activities. Depending on our customer’s need, we provide support for lead registrants through the critical path to registration and beyond.

As a first step for companies considering the option of taking the role of lead registrant we recommend our lead registrant risk analysis.

If you have any questions, please contact us.