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While the microorganisms’ working context is being currently revised, the industry still emphasises the need for further improvements, highlighting:
- The need to improve the Biological Properties document
- The necessity to update validation rules and
- The importance of having a clear and consistent data entry format, including a clear distinction between how to manage “legacy dossiers” and newly submitted ones.
The next IUCLID release is planned for October 2025. It will include improvements to the user interface, picklist management, the functionality to use the same dataset for multiple recipients. The release will also include various bug fixes identified during the May update.
The IUCLID Report generator is in the testing phase until July 31. A consolidated version of the MRL report is planned to be introduced for endorsement in the ScoPAFF Section Phytopharmaceutical – Residues around November 2025. For further details, please view the meeting minutes.
Our regulatory teams are experienced in the preparation of IUCLID dossiers for plant protection products, chemicals, biocides and microorganisms and actively involved in the EFSA steering committee, thus closely following the changes in data requirements.
Feel free to contact us if you would like to submit IUCLID dossiers for your active substances, microorganisms, maximum residue levels (MRLs) or import tolerance applications, and/or if you are interested in learning more about the recent developments. We can support you with all issues related to preparing or submitting the dossiers.
