CEPRA for Chemicals Testing

Toxicological Test

CEPRA proposes TOXICOLOGICAL TEST according to GLP (Good Lab Practice) as required by REACH Regulation 1907/2006 or by GHS

Thanks to a national and international labs, CEPRA support the company to choose best testing strategy, the best lab and to evaluate results of studies

Principal TOXICOLOGICAL TEST / STUDIES:

ANNEX

Number

STUDY

GUIDELINE

VII 8.1 Skin irritation / corrosion (in vitro) OECD 431 – OECD 439
VII 8.2 Eye irritation / corrosion (in vitro) OECD 437 – OECD 492
VII 8.3 Skin sensitization OECD 429
OECD 406, EEC B.6
OECD 442
VII 8.4.1 Bacterial reverse mutation test (Ames-test) OECD 471- EEC B.13/ 14
VIII 8.4.2 Cytogenetic testing in mammalian cells:
Chromosome Aberration Test (in vitro)
OECD 473
EEC B.10
VIII 8.4.2 Micronucleus test (in vitro) OECD 487
EEC B.10
VIII 8.4.3 Gene mutation test in mammalian cells:
Mouse Lymphoma Assay (in vitro)
OECD 476
EEC B.17
VII 8.5.1 Acute oral toxicity
– Acute Toxic Class Method “ATC”
– Fixed dose procedure
– Up and down procedure
OECD 423
OECD 420
OECD 425
VIII 8.5.2 Acute inhalation toxicity OECD 403
VIII 8.5.3 Acute dermal toxicity OECD 402, OECD 434
EEC B.3
Repeated dose toxicity OECD 40 -EEC B.7
OECD 410
OECD 412
OECD 408 – EEC B.26
OECD 411
OECD 413
OECD 452
VIII 8.8.1 Assessment of the toxicokinetic behaviour OECD 417