Evidence map›Paper›PMID 42460044›Full record

ArticleFrontiers in bioengineering and biotechnology2026

Closing the implementation gap: a harmonised EU framework for synthetic nucleic acid screening and customer verification.

Sophie Peresson, Patrick Stadler

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Sophie PeressonIndependent Consultant, Paris, France.
Patrick StadlerPour Demain, Bern, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synthetic nucleic acid technologies underpin modern biological research and biomanufacturing. However, their growing accessibility through commercial synthesis services, benchtop devices, and AI-assisted design tools creates significant dual-use biosecurity risks. This paper presents a harmonised EU biosecurity screening framework operationalised through the proposed EU Biotech Act I (December 2025), evaluating two complementary control mechanisms: Know Your Customer (KYC) verification and sequence screening against Sequences of Concern (SOC). We find that existing voluntary frameworks leave systematic coverage gaps that binding EU-level obligations, anchored to ISO 20688-2:2024, would substantively address - particularly for smaller providers and benchtop devices. We argue that near-term EU action offers a time-sensitive opportunity to shape global synthetic biology governance before regulatory fragmentation becomes entrenched.

Indexed as

biosecurityknow your customer (KYC) verificationregulationsequence screeningsequences of concern (SOC)

Identifiers

PMID42460044
PMCPMC13370156

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.