Our quality standards

Good Clinical Laboratory Practice (GCLP)

For projects supporting clinical trials, OHMX.bio adheres to GCLP standards for specific pipelines. This compliance ensures that our laboratory practices, from sample handling and analysis to data reporting, meet the necessary requirements for clinical-grade sequencing and biomarker studies, providing the reliability essential for regulatory submissions and clinical decision-making. 
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ISO Certifications

OHMX.bio operates under a robust quality management system, certified to ISO 9001, ensuring consistent quality in all our processes and services. Furthermore, our commitment to data security and confidentiality is demonstrated by our ISO 27001 certification, which governs the protection of your sensitive data throughout its lifecycle. 

Good Manufacturing Practice (GMP)

While OHMX.bio currently focuses on research and GCLP-compliant services, we are actively working towards expanding our capabilities. We expect to offer analysis for specific biologics quality control under GMP guidelines starting in 2026. In the interim, we leverage the extensive expertise of our sister-entity, Anabiotec, which already provides a broad spectrum of GMP-compliant solutions, allowing us to support clients with diverse regulatory needs through a collaborative approach.
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General Data Protection Regulation (GDPR)

We prioritize the privacy and protection of all data entrusted to us. OHMX.bio is fully compliant with the GDPR, implementing robust measures for data collection, processing, storage, and transfer. This ensures that sensitive personal and research data are handled with the highest level of security and in accordance with strict privacy regulations.

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