What we do

The Transparency and Reproducibility Committee works to strengthen trust in pharmacological research by promoting rigorous, verifiable, and well-documented scientific practices. Its role is to support a research ecosystem where results can be confidently interpreted, reused, and built upon by the global scientific community.

What we do

The Transparency and Reproducibility Committee works to strengthen trust in pharmacological research by promoting rigorous, verifiable, and well-documented scientific practices. Its role is to support a research ecosystem where results can be confidently interpreted, reused, and built upon by the global scientific community.

Improving Transparency and Reproducibility in Preclinical Research

The IUPHAR Transparency and Reproducibility Subcommittee (Basic and Translational Section) is promoting an Open Access database, which gives information on free online resources that help to guide good practice in preclinical research, especially in respect of experiments that use animals.

Topics addressed by these resources include: planning experiments (PREPARE); designing experiments (the ‘EDA’); statistical analysis of the data (InVivoStat); reporting the experimental findings (ARRIVE 2.0); 3Rs compliance; and optimizing research animal welfare. Good practice in all these and other aspects of preclinical research will help to improve both reproducibility of research findings and their successful translation.

We strongly encourage members to use the resources listed in the database and to share the link with their contacts. Also, we welcome receiving information on online resources that could be added to the database. Please send any suggestions to d.i.lewis@leeds.ac.uk .

Improving Transparency and Reproducibility in Preclinical Research

The IUPHAR Transparency and Reproducibility Subcommittee (Basic and Translational Section) is promoting an Open Access database, which gives information on free online resources that help to guide good practice in preclinical research, especially in respect of experiments that use animals.

Topics addressed by these resources include: planning experiments (PREPARE); designing experiments (the ‘EDA’); statistical analysis of the data (InVivoStat); reporting the experimental findings (ARRIVE 2.0); 3Rs compliance; and optimizing research animal welfare. Good practice in all these and other aspects of preclinical research will help to improve both reproducibility of research findings and their successful translation.

We strongly encourage members to use the resources listed in the database and to share the link with their contacts. Also, we welcome receiving information on online resources that could be added to the database. Please send any suggestions to d.i.lewis@leeds.ac.uk .

Who we are

Chair
Clare Stanford
Clare Stanford

United Kingdom

Deputy Chair
Mike Curtis
Mike Curtis

United Kingdom

Member
Amrita Ahluwalia
Amrita Ahluwalia

United Kingdom

Member
Christopher George
Christopher George

United Kingdom

Member
Debbie Hay
Debbie Hay

New Zealand

Member
Simon Bate
Simon Bate

United Kingdom

Member (Early Career Researcher)
Farhad Dehkhoda
Farhad Dehkhoda

Australia

Councilor
John Kolassa
John Kolassa

United States

Councilor
Michael Spedding
Councilor
Taiwo Omotoso
Taiwo Omotoso

Nigeria

Councilor
Vandana Nikam
Councilor
Vanessa Minervini
Vanessa Minervini

United States

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