Biocides registration service

Our team has undertaken and successfully completed dozens authorization of biocidal products worldwide. We are ready to listen to your needs and design the right strategy to achieve full enrollment and authorization.

To help you comply with regulations, we performed an action plan six steps that cover all aspects of registration and approval of national products.

1.) Determining the scope of the evaluation
Confirmation that the product is within the scope of Regulation 528/2012

2.) Assessment of registrability
Data search and analysis of regulatory trends and possibilities

3.) Analysis of available data
Assessment data against data requirements, evaluation strategy and cost estimation

4.) Fill the gaps identified in data analysis
Statements, exemptions or studies

5.) Dossier preparation (including hazards, exposure and risk assessment)
Summaries, IUCLID5 and R4BP

6.) Dossier submission and subsequent monitoring
meetings with regulatory authorities and project review

These services can be provided by project or project for the complete management of a presentation to final approval.

Additional services include expert advice on classification and labeling, risk assessments (occupational and environmental), discussion and negotiations with the authorities, project management and monitoring of study.

We are ready to discuss your requirements.

Project management
Strategy Register
Dossier compilation in CADDY, IUCLID5, RRA or R4BP
Analysis of data breaches
Monitoring Study
Proposed classification and labeling according to CLP
Determination of endocrine disrupters
Human risk and exposure assessment
The environmental risk assessment and exposure
Writing technical file
Support post-presentation