https://en.bioecon.ru/companies/eurofins/Recent content in Eurofins on BioeconHugoen-USSun, 26 Jul 2026 00:23:48 +0700https://en.bioecon.ru/technology/fsma-haccp-certification-for-bio-food/Sat, 25 Jul 2026 17:10:00 +0000https://en.bioecon.ru/technology/fsma-haccp-certification-for-bio-food/Third-party audit, certification and testing that lets a food business prove its safety system works — FSMA Section 204 traceability with key data elements and critical tracking events, the FSSC 22000 Version 7 transition running to May 2027, HACCP preventive controls, and the laboratory verification underneath all of it.https://en.bioecon.ru/technology/novel-food-approval-as-a-service-eu-uk-sg/Sat, 25 Jul 2026 17:00:00 +0000https://en.bioecon.ru/technology/novel-food-approval-as-a-service-eu-uk-sg/Consultancies that carry a new food ingredient through pre-market authorisation — EFSA novel food dossiers, UK FSA filings that no longer follow the EU automatically, US GRAS notifications and Singapore submissions — a service defined by the fact that the same ingredient now needs separate dossiers per jurisdiction.https://en.bioecon.ru/technology/dna-synthesis-gene-foundry/Thu, 23 Jul 2026 00:00:00 +0000https://en.bioecon.ru/technology/dna-synthesis-gene-foundry/The commercial gene-synthesis service and biofoundry layer of synthetic biology — turning digital DNA designs into delivered genes, clones and strain builds through phosphoramidite and emerging enzymatic synthesis, governed by pathogen-sequence biosecurity screening.https://en.bioecon.ru/technology/toxics-screening-toxicomics-service/Wed, 22 Jul 2026 00:00:00 +0000https://en.bioecon.ru/technology/toxics-screening-toxicomics-service/Contract safety assessment that takes a drug candidate from in-silico ADMET triage through in-vitro panels (hepatotoxicity, hERG, CYP induction) to GLP in-vivo studies, delivering the IND-enabling toxicity package regulators require — now augmented by toxicogenomics and virtual control groups.https://en.bioecon.ru/technology/process-validation-qualification-cro/Mon, 06 Jul 2026 00:00:00 +0000https://en.bioecon.ru/technology/process-validation-qualification-cro/CRO-delivered three-stage process validation and IQ/OQ/PQ qualification of biopharma equipment — media fills, cleaning validation, CSV and viral clearance under FDA/EudraLex Annex 1 cGMP.https://en.bioecon.ru/technology/one-health-zoonosis-amr-monitoring/Tue, 30 Jun 2026 00:00:00 +0000https://en.bioecon.ru/technology/one-health-zoonosis-amr-monitoring/Outsourced One Health surveillance that fuses veterinary, human and environmental sampling with shotgun metagenomic sequencing, CARD resistome profiling and AI spillover-risk scoring to detect zoonotic pathogens and antimicrobial resistance, delivered as an ISO 17025 reference-lab service under EU 2003/99/EC, US NARMS and China’s containment plan.