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Nominations and Submissions

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A test method submission consists of a proposal to ICCVAM for consideration of a test method for which adequate validation studies have been completed to characterize the usefulness and limitations of the test method for a specific proposed regulatory requirement or application. Test method submissions require that adequate documentation of the scientific validity has been prepared in accordance with ICCVAM test method submission guidelines.

A test method nomination consists of a proposal to ICCVAM for review and evaluation for which a complete test method submission is not available. Four examples are:

  • Test methods for which adequate validation studies presumably have been completed but lack a complete submission package
  • Test methods that appear promising based on limited prevalidation or validation data and are proposed for additional validation studies
  • Test methods that have been developed and are proposed for prevalidation or validation studies
  • Test methods that are recommended for a workshop or other activity

Test method nominations and submissions may be made via the NTP Online Nomination Form or by contacting NICEATM/ICCVAM.

Proposed test method nominations or submissions received by ICCVAM are initially assessed by NICEATM as to the relevance of the nomination or the adequacy and completeness of the submission. ICCVAM then determines the priority the proposed test method will have for technical evaluation. Once a proposed test method has been accepted for evaluation, ICCVAM assembles an interagency working group of government scientists with scientific and regulatory expertise in the appropriate scientific disciplines to collaborate with NICEATM on the evaluation process. Depending on the validation status of the proposed test method, ICCVAM, in conjunction with NICEATM, develops recommendations and priorities for further efforts. Such efforts might include an expert workshop, an expert panel meeting, a peer review meeting, an expedited peer review process, or a validation study.

Test method sponsors are encouraged to consult with NICEATM and ICCVAM throughout the test method development, prevalidation, and validation process, as well as during preparation of submissions. The objective of these interactions is to maximize the likelihood that validation studies and submissions will adequately characterize the usefulness and limitations of the proposed test method. Complete submissions are essential and serve as a basis for assessing the validation status of a proposed test method through an independent ICCVAM peer review process. This interactive process enhances the likelihood that agencies will have sufficient data and information to determine the extent that a test method can generate information that will meet their regulatory needs.


NICEATM/ICCVAM Guidelines for the
Nomination and Submission of New, Revised, and Alternative Test Methods

NIH Publication No. 03-4508
September 2003

Note: This document replaces the Evaluation of the Validation Status of Toxicological Methods: General Guidelines for Submissions to ICCVAM (NIH Publication No. 99-4496; rev. Oct. 20, 1999)

Document availability announced in Federal Register
View notice (Vol. 68, No. 220, pp. 64636, Nov. 14, 2003) [PDF]

List of Nominations

Nominator Nominated Test Method Activity Activity
Status
Additional
Materials
(Redacted at nominator's request) NTP Two-Year Toxicology and Carcinogenesis Rodent Studies [PDF] Under Consideration -
CPSC CPSC Nomination: Request for Assessment of the Validation of the Local Lymph Node Assay for Classification of Sensitizers [PDF] Under Evaluation List of References
HSUS Alternative Methods to Replace the Mouse LD50 Assay for Botulinum Toxin Potency Testing [PDF]

View HSUS Letter to Allergan, Inc. (Dec. 15, 2005) [PDF]
Workshop Completed List of References
CertiChem, Inc MCF-7 Estrogenic Activity Cell Proliferation Assay
View Nomination Cover Letter [PDF]
View Documentation Provided with Nomination [PDF]
Recommended for Validation Studies Pre-Screen Evaluations
Xenobiotic Detection Systems LUMI-CELLTM Estrogen Receptor HIgh-Throughput System for Screening Estrogen-Like Chemicals for Validation Studies
View Nomination Cover Letter [PDF]
View Documentation Provided with Nomination [PDF]
Validation Study Ongoing -

List of Submissions

Sponsor Test Method Evaluation
Status
Additional
Materials
Alternatives Testing Steering Committee:
Johnson Diversey
S.C. Johnson & Son, Inc.
The Procter & Gamble Company
The Accord Group
In Vitro Test Method for Assessment of the Eye Irritation Potential of Antimicrobial Cleaning Products

View Submission Cover Letter from IIVS, Inc. [PDF]

Under Evaluation -
ECVAM In Vitro Pyrogenicity Test Methods [PDF] Peer Review Complete Pyrogenicity Test Methods

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