CE
CE
We provide end‑to‑end support in the registration and certification of all categories of EU fertilising products covered by Regulation (EU) 2019/1009, including:
With CE marking, these products can be placed on the market across the entire European Union without the need to undergo separate national approval procedures.
New: CE Marking for Detergents
Soon, detergents will also fall under the mandatory CE‑marking requirements. CHEMLEX is already preparing its clients for this regulatory shift by providing requirement assessments and early‑stage documentation development.
We provide support in achieving compliance for fertilising products in the European Union in accordance with Regulation (EU) 2019/1009 of the European Parliament and of the Council of 5 June 2019, which lays down rules on the making available on the market of EU fertilising products, amends Regulations (EC) No 1069/2009 and (EC) No 1107/2009, and repeals Regulation (EC) No 2003/2003.
The Regulation establishes harmonised rules for placing fertilisers, plant biostimulants and other fertilising products on the EU market. It defines the quality, safety, composition, labelling and conformity‑assessment requirements that must be met for a product to bear the CE marking.
How can CHEMLEX support you?
We provide comprehensive advisory services that help you understand and effectively implement the requirements of Regulation (EU) 2019/1009.
We guide you through the entire process — from product assessment to final CE marking.
Our support includes:
Conformity Assessment Modules — how we support you
We prepare the complete technical documentation in line with the applicable conformity‑assessment module, assist in obtaining the CE mark, and manage communication with the notified body.
With CE marking, products can be placed on the market throughout the entire European Union without the need to undergo separate national approval procedures.
We provide with product registration according to the following modules:
This module requires documentation demonstrating the product’s conformity, but does not involve any interaction with a notified body.
Application of internal production control and supervised product testing (Module A1)
This module requires technical documentation demonstrating product compliance, mandatory engagement with a notified body, and testing performed by an accredited laboratory (including, where applicable, detonation‑resistance testing).
This pathway requires documentation demonstrating the product’s conformity and includes mandatory interaction with a notified body.
Application of production process quality assurance (MODULE D1)
This module requires documentation demonstrating the product’s conformity and involves mandatory interaction with a notified body, including a production‑site audit.
Why choose us?
