Regulatory Assessments

What do Factlines’ regulatory assessments cover?

Factlines' regulatory assessments focus on compliance with national and international laws related to sustainability, human rights, and procurement. These questionnaires help you document compliance, meet tender requirements, and respond to changing legislation.

Each supplier assessment can be tailored to frameworks such as the Norwegian Transparency Act, Corporate Sustainability Due Diligence Directive (CSDDD), Modern Slavery Act, and EU Deforestation Regulation (EUDR).

Essential for companies operating in regulated markets or public procurement.

Automatic risk scoring

Smart Follow-Up suggestions

AI summary and evaluation

Suppliers can reuse responses

Support for chain surveys

Overview of

Regulatory Assessments

Medisinteknisk utstyr

Assess key regulatory requirements for suppliers of medical devices. The questionnaire covers key requirements of the EU Medical Device Regulation (MDR 2017/745) and In Vitro Diagnostic Regulation (IVDR 2017/746), as well as chemical products, substances and mixtures.

The-Norwegian Transparency Act

Conduct complete supplier due diligence in line with the Norwegian transparency act. The assessment covers company policies, management systems, risk assessments, supply chain follow-up, labour rights, environmental practices, and anti-bribery and corruption.

EUs avskogingsforordning

The EU has introduced the EU Deforestation Regulation (EUDR) to ensure that products placed on or exported from the EU market do not contribute to the destruction of the world’s forests. Use this questionnaire to assess if your suppliers have the necessary systems and information in place to comply with the EU Deforestation Regulation.

Regulatory supplier assessments explained: what they cover and how to choose the right one

What do Factlines’ regulatory assessments cover?

Overview of

Regulatory Assessments

Medisinteknisk utstyr

The-Norwegian Transparency Act

EUs avskogingsforordning

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