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Test SubContracting
Groenakker offers a full suite of in vitro and in vivo services through qualified partners. We routinely assist clients by leveraging our global testing network to provide high-quality testing at industry-leading prices and turn around times. The most common studies which we support are available within the Shop, though through our partners we have access to the full compliment of biocompatibility tests associated with ISO 10993 and ISO 18562.
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How it works 
Test Sourcing
ISO 13485:2016 Quality Management System
We identify, qualify, and manage competent laboratory service providers so you don't have to.
Groenakker partners with ISO 17025 laboratory testing partners around the world to provide the best services at competitive prices and turnaround times. Along with chemistry and toxicology services provided through our ChemTox™ program, routinely subcontracted studies are listed below. If you do not see what you're looking for contact us today for a custom estimate.
Groenakker partners with ISO 17025 laboratory testing partners around the world to provide the best services at competitive prices and turnaround times. Along with chemistry and toxicology services provided through our ChemTox™ program, routinely subcontracted studies are listed below. If you do not see what you're looking for contact us today for a custom estimate.
How it works
Cytotoxicity
(ISO 10993-5)
Assesses the potential of a medical device material or extract to cause cell damage or death through in vitro cell culture testing.
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Sensitization
(ISO 10993-10)
Evaluates the potential of a medical device or its materials to induce an allergic response following exposure.
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Irritation
(ISO 10993-23)
Assesses the potential of medical devices and their materials to cause local irritation at the site of contact.
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Systemic Toxicity
(ISO 10993-11)
Examines the potential for systemic adverse effects resulting from exposure to medical device materials or their extracts throughout the body.
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Haemocompatibility
(ISO 10993-4)
Evaluates the interactions between medical device materials and blood to identify risks such as thrombosis, hemolysis, or adverse effects on blood components.
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Implantation
(ISO 10993-6)
Evaluates the local biological response of living tissues to medical device materials following implantation.
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