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Myeloid U937 Skin Sensitisation Test

Test Method Number: TM2013-02 (EU)
Short Name of TM: U-SENS™
Responsible Organisation: EURL ECVAM - European Union
General Comments: The U-SENS™ test method was formely called Myeloid U937 Skin Sensitisation Test (MUSST) (TM 2009-05).
Stage of Submission: Assessment Finalised
Stage of Validation: Finalised
Stage of Peer-review: Finalised
  • 1
    Submission
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    Validation
  • 3
    Peer-review
  • 4
    Recommendation
  • 5
    Regulatory acceptance/Standards

Myeloid U937 Skin Sensitisation Test

Test Method Number: TM2009-05 (EU)
Short Name of TM: MUSST
Responsible Organisation: EURL ECVAM - European Union
General Comments: Validation stopped. New submission with new protocol received under TM2013-02 (U-Sens)
Stage of Submission: Not considered for validation
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    Submission
  • 2
    Validation
  • 3
    Peer-review
  • 4
    Recommendation
  • 5
    Regulatory acceptance/Standards

Porcine corneal opacity reversibility assay

Test Method Number: TM2008-03 (EU)
Short Name of TM: PorCORA
Responsible Organisation: EURL ECVAM - European Union
General Comments: On hold-pending further information
Stage of Submission: Assessment Finalised
  • 1
    Submission
  • 2
    Validation
  • 3
    Peer-review
  • 4
    Recommendation
  • 5
    Regulatory acceptance/Standards

Prediction of the in vivo estrogenic activity of chemicals ERalpha-CALUX

Test Method Number: TM2009-11 (EU)
Short Name of TM: ERalpha-CALUX
Responsible Organisation: EURL ECVAM - European Union
General Comments: Not prioritised for validation by ECVAM. External validation performed.
Stage of Submission: Not considered for validation
Stage of Regulatory acceptance/Standards: Published
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    Submission
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    Validation
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    Peer-review
  • 4
    Recommendation
  • 5
    Regulatory acceptance/Standards

Rat recombinant androgen receptor binding assay for the detection of compounds with (anti)androgenic potential

Test Method Number: TM2010-01 (EU)
Short Name of TM: ARBA
Responsible Organisation: EURL ECVAM - European Union
General Comments: Not prioritised for validation by ECVAM
Stage of Submission: Not considered for validation
  • 1
    Submission
  • 2
    Validation
  • 3
    Peer-review
  • 4
    Recommendation
  • 5
    Regulatory acceptance/Standards

RHE IL-18 potency test for skin sensitization

Test Method Number: TM2012-05 (EU)
Short Name of TM: RHE IL-18
Responsible Organisation: EURL ECVAM - European Union
General Comments: Invitation to send a full submission
Stage of Submission: Assessment of Pre-submission
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    Submission
  • 2
    Validation
  • 3
    Peer-review
  • 4
    Recommendation
  • 5
    Regulatory acceptance/Standards

SENS-IS

Test Method Number: TM2011-11 (EU)
Short Name of TM: SENS-IS
Responsible Organisation: EURL ECVAM - European Union
General Comments: Under external validation
Stage of Submission: Assessment Finalised
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    Submission
  • 2
    Validation
  • 3
    Peer-review
  • 4
    Recommendation
  • 5
    Regulatory acceptance/Standards

Skin absorption based on RHE models

Test Method Number: TM2008-13 (EU)
Short Name of TM: Skin absorption RHE
Responsible Organisation: EURL ECVAM - European Union
General Comments: On hold-pending further information
Stage of Submission: Assessment of Pre-submission
  • 1
    Submission
  • 2
    Validation
  • 3
    Peer-review
  • 4
    Recommendation
  • 5
    Regulatory acceptance/Standards

Skin Irritation Test for the Prediction of Acute Skin Irritation of Chemicals With Sterlab RHE: 42 minutes application + 42 hours post-incubation

Test Method Number: TM2014-06 (EU)
Short Name of TM: Sterlab RHE SIT
Responsible Organisation: EURL ECVAM - European Union
General Comments: Further clarifications requested
Stage of Submission: Assessment Finalised
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    Submission
  • 2
    Validation
  • 3
    Peer-review
  • 4
    Recommendation
  • 5
    Regulatory acceptance/Standards

Skin PAMPA Permeability System

Test Method Number: TM2012-02 (EU)
Short Name of TM: Skin PAMPA
Responsible Organisation: EURL ECVAM - European Union
General Comments: Validation on hold. Considered to be followed up in the wider context of ADME methods
Stage of Submission: Assessment of Full submission
  • 1
    Submission
  • 2
    Validation
  • 3
    Peer-review
  • 4
    Recommendation
  • 5
    Regulatory acceptance/Standards