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FRANCOPA is the French platform dedicated to development, validation, and dissemination of alternative methods in animal testing. It was created on July 6th 2007 at an inaugural meeting at the Ministry of Research. The platform gathers all French partners on the same aim to promote the development of alternative methods for the reducing or the replacement of animal testing, particularly in the development, the evaluation, and control of health products and chemicals.

FRANCOPA is a member of the European platform (European Consensus-Platform for Alternatives).

FRANCOPA is composed of fifteen partners representing governmental institutions, academic research, industry, and nongovernmental organisations for animal care groups.
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The activities have been centered initially on the establishment of a state of the art on 3R methods and practices in France (English table), together with recommendation to the French government.

GIS report for the Ministry of Research abstract

more (french version)...

Applying and recommendation in international seminar was held on waiving animal testing for regulatory purposes.

FRANCOPA Workshop report - Paris, sept 1st, 2011 - Waiwing animal testing for regulatory purposes

Together with the SFT and the SPTC, FRANCOPA organised a seminar on read-across in Paris, 15th November 2013. A summary and a position letter were subsequently written by FRANCOPA.

Summary of the seminar on read-across (french version)

Position letter on read-across by FRANCOPA

FRANCOPA info-center aims at facilitating the sharing and exchanges of information and opinions among people involved in the development or promotion of alternative methods in animal testing. It is an interactive website with the following sections :
• Database with a searching engine (data from FRANCOPA and associated websites).
• Discussion forum.
• Newsletter, twice a year, related to methodological advances and FRANCOPA actuality.
• Frequently Asked Questions.
• Links to related websites.



with support from
News
01/09/2016 - 16/12/2016
Good In Vitro Method Practices
The Draft Guidance Document on Good In Vitro Method Practices (Givimp) for the Development and Implementation of In Vitro Methods for Regulatory Use in Human Safety Assessment is open for public comments


08/11/2016
Latest EURL ECVAM Status Report published
EURL ECVAM Status Report on the Development, Validation and Regulatory Acceptance of Alternative Methods and Approaches (2016)


21/11/2016 - 23/11/2016
"Le droit de l'animal"
Formation "Le droit de l'animal" à l'Université de Strasbourg


15/02/2017 - 16/02/2017
Workshop, London
Applying exposure science to increase the utility of non-animal data in efficacy and safety testing


14/06/2017 - 16/06/2017
ecopa - SSCT Workshop, Helsinki
Up-to-date in vitro approaches in regulatory risk assessment and disease modelling