Chemical regulatory and compliance reports

Designed by regulatory experts to support organisations with maintaining compliance by providing a consolidated view of changes and updates, our reports save you time, and condense complex legalities into accessible, easily digestible outputs.

Distributed proactively when regulatory updates are announced or adopted, our reports provide you the maximum opportunity to make strategic decisions and can be tailored to the specific requirements of your product portfolio and trade markets. 

Reports

While we offer a number of standard reports, we can also provide tailored solutions for your exact requirements.

EU Poison Centre Compliance Report

Compiled by our Poison Centre experts, this report supports customers by providing an overview of Poison Centre information in the EU and European Economic Area (EEA), the United Kingdom, and Switzerland. Including:

• An overview of Article 45 and Annex VIII to CLP
• What changes Annex VIII has brought to Poison Centre notification such as:
  
  • the introduction of UFI’s (Unique Formula Identifiers)
  • the European Product Categorisation System
  • workability solutions
• The status of each member-state including:
  
  • whether they are accepting notification via the ECHA portal
  • if there are additional actions that must be completed outside of the ECHA portal
  • the Poison Centre phone numbers and the conditions of use.

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Global Poison Centre Compliance Report

Detailing Poison Centre requirements globally, this report supports organisations to understand their obligations outside of Europe, the United Kingdom & Switzerland by providing an overview of:

• which countries have Poison Centre obligations.
• which countries have published intentions to implement Poison Centre notifications in the future.
• which countries do not currently require a Poison Centre Notification.
• the Poison Centre phone numbers for each country and the conditions of use.  

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Biocide Report

The Biocidal Product Regulation (BPR) (Regulation (EU) 528/2012) concerns the use and placement of biocidal products in the EU market. This report provides an overview of:

• general requirements for Biocidal Product Authorisation
• active Substance Approval Process – Stage 1
• biocidal Product Authorisation – Stage 2
• differences between EU BPR and GB BPR
• member-state analysis for National Registration 

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SCIP Notification Report

SCIP is the database for information on ‘Substances of Concern In articles as such or in complex objects (Products)’ and was established under the EU’s Waste Framework Directive (WFD) due to concerns on the presence of hazardous chemicals in items that may be repurposed under the principles of a circular economy.  

Companies supplying the EU market with articles containing substances of very high concern (SVHC) on the Candidate List at a concentration above 0.1% weight by weight are required to submit information to ECHA.

Supporting organisations to understand the SCIP regulation and their requirements, the report provides:

• Guidance on the SCIP regulation
• General requirements for SCIP registrations
• Guidance on how to complete SCIP registrations

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