End-to-end support
From biological evaluation to substance-based Medical Devices, we offer integrated testing and advisory services.
Biological Safety
Substance-Based MD
Advisory
Top reasons customers test with us: Scientific expertise and personal support
Meet Your Deadlines with Confidence.
+25 years of in vitro science expertise
Specialized in difficult-to-test samples
Personal support throughout your project
GLP compliant laboratory
SenzaGen meets the GLP requirements set by the OECD.
GLP stands for Good Laboratory Practice and is a quality system of requirements and principles to assure the quality of non-clinical safety studies. What constitutes GLP is defined by the OECD for use as a global standard requirement to ensure high-quality and reliable results for product filings and regulatory approval.
Swedac, the Swedish national accreditation body, is the authority that has determined that SenzaGen’s lab meets the GLP requirements.
Benefits of GLP
- Traceability of study data
- Compliant archiving of study documents
- Compliance with regulatory requirements
We help you through challenges in your product life cycle
