At Versa Biomedical, quality is not just a step in the process, it is the foundation of everything we do. From how we design studies to how we support our clients, every project is guided by the highest standards of precision and reliability.

After recently obtaining the ISO 13485 certification, which recognizes compliance with international quality standards for medical devices. and being acknowledged as a GLP-compliant preclinical research center, we now add a new milestone: the ISO 9001 certification.

This achievement strengthens what we call our Triple Quality framework:
ISO 13485 – Quality for medical device development
GLP – Good Laboratory Practices for regulated, secure research
ISO 9001 – Organization-wide quality management

This triple certification places Versa Biomedical among a small group of preclinical CROs able to offer this level of regulatory and technical assurance. It is a signal of trust for our clients and a testament to our deep commitment to rigor, traceability, and scientific excellence.

But beyond the recognition, it is about purpose: enabling open biomedical models, expanding possibilities, and supporting those who drive innovation in health.

At Versa Biomedical, every step forward in quality is a step toward our purpose:
Open models. Open futures.