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EU Parl Watch

Changes between two versions

What changed between the plenary report and the adopted text

From · plenary report· 14 Nov 2025

A-10-2025-0234

on ensuring the faster registration and uptake of biological control agents

To · adopted text· 25 Nov 2025

TA-10-2025-0284

Ensuring faster registration and uptake of biological control agents

AI:What changed, in short

The versions differ only in formal points: punctuation and number formatting are corrected.12

0 changes of substance · 2 formal · 0 of wording only

Written by AI from the two texts only · read the changes before relying on it · 4 Sept 2026 · Report a problem

Changes to the text itself, in document order. Cover page, citations and punctuation-only edits are left out; they are under “Every difference”.

Changes of substance · 0

None: the changes are formal or of wording only.

2 formal changes: legal basis, citations, references, corrections

Change 1 Formal

AI summary:Fixes punctuation: replaces a hyphen with a period after the initial 'I'.

Show the text change (1 line)

Changed:II. whereas the fast-track processing and placing on the EU market of biological control would increase availability and provide an opportunity to combat the resistance of pests and diseases to current PPPs; whereas this would help to promote more sustainable agricultural practices and increase the resilience and competitiveness of the agricultural sector by keeping the farmers’ toolbox of pest control options as broad as possible;

Change 2 Formal

AI summary:Changes the decimal separator in the amount from a period to a comma, aligning with European formatting.

Show the text change (1 line)

Changed:M. whereas EU-based small and medium-sized biocontrol enterprises represent approximately 70 % of the EU biocontrol sector; whereas these companies are key drivers of sustainable innovation; whereas the approval of active substances for PPPs, including biological control agents in the EU, entails significant costs, with overall investment, including data generation, regulatory fees and national authorisations, estimated at between EUR 1.51,5 and EUR 4 million per substance;