Standard regulatory tests under GLP
We carry out regulatory genotoxicity and (cyto)toxicity analysis as part of a battery of tests which can be adapted according to your needs, your product and according to regulatory requirements or the stage of development of your product.
| REGULATORY TESTS | DOCUMENTS (FR) | DOCUMENTS (EN) |
|---|---|---|
| Bacterial Gene mutation test (Ames test) | OCDE 471 | OECD 471 |
| In vitro chromosome aberration test on mammalian cells | OCDE 473 | OECD 473 |
| In vitro gene mutation test in L5178Y mouse lymphoma cells (MLA/TK) or in human TK6 cells | OCDE 490 | OECD 490 |
| In vitro micronucleus test in mammalian cells | OCDE 487 | OECD 487 |
| In vitro skin irritation: reconstituted human epidermis test method | OCDE 439 | OECD 439 |
| In vitro skin corrosion: human skin model test | OCDE 431 | OECD 431 |
| Bhas 42 cell transformation test (according to ENV/JM/MONO [2016]1) | ||
| Cytotoxicity test by MTT or neutral red method (biomaterials) (according to NF EN 30993-5/ISO 10993-5) | ||
| Bone marrow micronucleus in vivo test | OCDE 474 | OECD 474 |
| In vivo comet assay | OCDE 489 | OECD 489 |
| Acute toxicity – acute toxic class method | OCDE 423 | OECD 423 |
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