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Prenumeration

Kalender

Est. tid*
2026-02-13 08:30 Bokslutskommuniké 2025
2025-11-05 - Kvartalsrapport 2025-Q3
2025-08-20 - Kvartalsrapport 2025-Q2
2025-05-15 - X-dag ordinarie utdelning SENZA 0.00 SEK
2025-05-14 - Årsstämma
2025-05-14 - Kvartalsrapport 2025-Q1
2025-02-13 - Bokslutskommuniké 2024
2024-11-08 - Kvartalsrapport 2024-Q3
2024-08-22 - Kvartalsrapport 2024-Q2
2024-05-16 - X-dag ordinarie utdelning SENZA 0.00 SEK
2024-05-15 - Årsstämma
2024-05-15 - Kvartalsrapport 2024-Q1
2024-02-14 - Bokslutskommuniké 2023
2023-08-24 - Kvartalsrapport 2023-Q2
2023-05-05 - X-dag ordinarie utdelning SENZA 0.00 SEK
2023-05-04 - Årsstämma
2023-02-16 - Bokslutskommuniké 2022
2022-08-18 - Kvartalsrapport 2022-Q2
2022-05-06 - X-dag ordinarie utdelning SENZA 0.00 SEK
2022-05-05 - Årsstämma
2022-02-11 - Bokslutskommuniké 2021
2021-08-19 - Kvartalsrapport 2021-Q2
2021-05-06 - X-dag ordinarie utdelning SENZA 0.00 SEK
2021-05-05 - Årsstämma
2021-02-18 - Bokslutskommuniké 2020
2020-08-20 - Kvartalsrapport 2020-Q2
2020-05-11 - X-dag ordinarie utdelning SENZA 0.00 SEK
2020-05-08 - Årsstämma
2020-02-13 - Bokslutskommuniké 2019
2019-12-18 - Extra Bolagsstämma 2019
2019-08-22 - Kvartalsrapport 2019-Q2
2019-05-16 - X-dag ordinarie utdelning SENZA 0.00 SEK
2019-05-15 - Årsstämma
2019-02-14 - Bokslutskommuniké 2018
2018-08-22 - Kvartalsrapport 2018-Q2
2018-05-09 - X-dag ordinarie utdelning SENZA 0.00 SEK
2018-05-08 - Årsstämma
2018-02-14 - Bokslutskommuniké 2017

Beskrivning

LandSverige
ListaFirst North Stockholm
SektorHälsovård
IndustriBioteknik
Senzagen är verksamt inom medicinteknik. Bolaget utvecklar och genomför genomiska in vitro-tester, vilket innebär att olika kemikaliers toxikologiska förmåga inte testas på djur utan istället i provrör. Bolaget har utvecklat en teknologisk plattform som används för att studera substansers påverkan producerat av aktörer inom läkemedel, kosmetika- och kemikalieindustrin. Verksamheten bedrivs från huvudkontoret i Lund.

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2025-12-16 07:30:00

SenzaGen continues to solidify its role as an important partner for customers with high safety testing requirements, securing an assignment worth approximately 1.5 MSEK from a leading American chemical company. This business is part of the strong order intake during the second half of the year, both strengthening SenzaGen's position in the US market and confirming the company's expertise in testing complex chemicals. The testing includes the company's proprietary non-animal method GARD®skin along with complementary testing methods and will be conducted at the company's GLP-certified laboratory in Lund, with the majority scheduled for 2025.

The chemical industry represents one of SenzaGen's most significant market segments. Substances in this sector are often hazardous and challenging to test, requiring reliable methods that deliver accurate results – an area where SenzaGen has established deep expertise and leading capabilities. This fall, the company has secured two major orders from US chemical companies while seeing increased activity across other US market segments, reinforcing its position in this strategic market.

"We've seen a notable increase in orders from US customers during the second half of the year, including the chemical industry. This development reflects the global shift away from animal testing while simultaneously strengthening our position in a strategically important market. It demonstrates that world-leading customers with complex testing needs are choosing our unique non-animal testing platform. Additionally, this order intake validates our strategic investment in expanding our test portfolio and confirms the competitiveness of our offering," says Peter Nählstedt, CEO and President of SenzaGen.

The testing includes GARD®skin, SenzaGen's proprietary non-animal method for skin sensitization testing, as well as complementary tests for additional regulatory endpoints. The GARD® technology leverages genomics and machine learning to generate highly reliable and accurate data for both pure chemicals and complex substances and mixtures that are traditionally difficult to test. The assay is approved for regulatory use by the OECD under Test Guidelines 442E and 497.

Demand for non-animal testing methods continues to accelerate as regulatory authorities worldwide advance initiatives to phase out animal testing. In the United States, both the FDA and NIH have signaled clear commitments to reducing reliance on animal testing, while UK authorities have recently announced similar initiatives.