SCIP Compliance Software

iPoint Compliance SCIP Connector automates the creation of SCIP dossiers and the exchange of data with ECHA`s new SCIP database.

Our SCIP Compliance Solution

 

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.

 

iPoint is member of the ECHA IT User Group

As a official member of the IT User Group we provide input on the development of the system, share our ideas for improvement,  analyse different scenarios and help to identify the areas where extra attention is needed in order to provide adequate support/guidance. Based on our extensive expert knowlegde we have developed a connector for the automated information exchange between ECHA’s SCIP database and iPoint Compliance.

 

iPoint's SCIP Connector

With the iPoint SCIP Connector we offer a system-to-system solution that allows a bulk upload of data to ECHA’s SCIP database.

 

• 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

 

> For the latest updates on SCIP please visit our blog that we frequently update

RoHS Compliance Software Benefits

Benefits

✔ Easy handling of large amounts of data


✔ Collection of all data in one place


✔ Collection of missing data

RoHS Compliance Software Features

Features

  • Automated analysis and reporting, bulk upload

  • Setting and managementof default values

RoHS Compliance Software Functionalities

Functionalities

  • Overview of completeness of dat

  • Task management and change management

  • Concise management of dossier information (incl. history and versions)

Videos
iPoint Compliance: SCIP Database Connector

See 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.

 

iPoint Compliance: Get ready for ECHA's SCIP database

Get an in-depth insight into SCIP database – What is required, and how you can get started with iPoint Compliance.

 

White Papers

 

 

 

 

SCIP Database Insights - Are you ready for SCIP reporting?

Be prepared for the upcoming challenges of the SCIP database

  

 

 

 

 

FAQ: The Echa SCIP Database

We have received a lot of questions on the upcoming SCIP Database. Here are the answers on the TOP 40 frequently asked questions.

 

Get in touch

Europe and Asia Pacific

Hans-Gerhard Lang

> Email

Phone +49 7121 14489 777

North America

Marc Church

> Email

Phone +1 248 282 4085

Trusted by companies of any size, in every industry, including
 
 
What is the SCIP database?

 

With the revision of the Waste Framework Directive (EU) 2018/851, Article 9, the European Chemicals Agency ECHA was tasked with the implementation of a database collecting (and making available) information on articles containing Substances of Very High Concern (SVHC) above 0.1% by weight as specified by the Candidate list.

 

ECHA has published a document detailing the information requirements  of the so-called SCIP database. Companies placing an article containing an SVHC above 0.1% on the EU market are required to submit information from January 5th, 2021 onwards. A first version of the SCIP database will be available one year prior to this date.

SCIP stands for Substances of Concern In articles, as such or in complex objects (Products). Although the SCIP acronym encompasses “products”, ECHA explicitly avoids using the term in the description of its information requirements limiting it to “articles”. Mixtures and substances are not under consideration, information obligations exist for articles as such as well as articles in complex objects.  (For a more detailed description see ECHA’s Guidance on requirements for substances in articles.)

Three key information constituents have to be provided

  1. article identification

  2. safe use information and

  3. identification, location, and concentration of the Candidate list substance(s) contained

> For the latest updates on SCIP please visit our blog that we frequently update