Watch a live demo of the iPoint Compliance SCIP Connector that automates the creation of SCIP dossiers and the exchange of data with ECHA`s new SCIP database.


Companies placing an article containing an SVHC above 0.1% on the EU market are required to submit information to the SCIP database from January 5th, 2021 onwards. With the majority of complex products containing SVHCs above 0.1% w/w, this requirement will impact most importers to and manufacturers within the European Union.


Sneak Peek at iPoint's SCIP Connector

  • Management of your company’s one or more ECHA UUIDs required for SCIP submission

  • Extensive options of default settings allowing easy initial SCIP reporting on the basis of existing data

  • Management of product details and setting of SCIP relevance

  • Dossier Creation, Validation and Upload

> Download the presentation
CARE 605x451

The CARE Principle

To achieve your company's sustainability and compliance goals, you need to control the complex and dynamic factors that impact them. iPoint provides the transparency you need to simplify compliance, sustainability and risk management.

This requires taking 4 steps: collect the relevant data and analyze the relations and impacts in order to report the right information to the relevant stakeholders and evolve the company towards your goals by minimizing risks and enabling collaboration and continuous improvement.

The CARE principle is the core of the iPoint Suite. By applying CARE, companies can, among other things, identify substances of concern or their product's carbon footprint, qualify and approve suppliers, and thus take control of their environmental, social and economic impacts.

iPoint supports you on the path to product compliance and decarbonization all the way.