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Francis P. Crawley

Francis P. Crawley is a philosopher specialized in research ethics, integrity, and methodology, and data/AI ethics & law. He is the Executive Director of the Good Clinical Practice Alliance – Europe (GCPA) and the Strategic Initiative for Developing Capacity in Ethical Review (SIDCER) in Leuven, Belgium. He coordinated the GCPA-SIDCER European Fellowship in Research Ethics (EFRE). He is Chairman of the EOSC Future / RDA Artificial Intelligence and Data Visitation Working Group & EOSC Future / RDA Ambassador for Ethics & Law. He also chairs the International Data Policy Committee of the International Committee on Data (CODATA), International Science Council (ISC). He recently founded the Ukraine Clinical Research Support Initiative (UCRSI). He has acted as an author or expert for the WHO and other leading international and European research ethics and GCP guidelines, as well as for several guidelines in Asia, Africa, the Americas, and Europe.
He is the past Secretary General, Ethics Officer, and Chairman of the Ethics Working Party at the European Forum for Good Clinical Practice. He chaired the methodologies sub-group of the Real Word Data Working Group at the Faculty of Pharmaceutical Medicine, Royal Colleges of Physicians, and sat for three years on their Ethics & Practice Committee. He is currently a member if the Ethics Working Group of the International Federation of Associations of Pharmaceutical Physicians and Pharmaceutical Medicine (IFAPP).
He was for 15 years the Chairman of the Ethics Review Committee of the International Network for Cancer Treatment and Research (INCTR); a member of the INCTR Tissues Committee; and a member of the Ethics Committee of the European Organization for Research & Treatment of Cancer; Consultant to the Peking University Institutional Review Board; and a member of the Steering Committee of the Chinese Ethics Committee of Registering Clinical Trials (ChECRCT). He has been a member of the joint EMVI-AMVTN Ethical Review Committee; a Permanent Liaison Officer to the International Bioethics Committee of UNESCO; and a Contact Officer for CIOMS. In 2006 he was Visiting Expert in research ethics at the Ministry of Health, Singapore.
He was the committee chairman of the WHO guidelines on ethics committees and data monitoring committees; and he was a member of the Scientific Advisory Committee for the World Health Organization’s International Clinical Trials Registry Platform (ICTRP). He also served for four years on the UNAIDS Ethical Review Committee. He is a co-founder and past Steering Committee Member of the Global Forum for Bioethics in Research; a past member of the Committee of Interested Parties of the Centre for the Management of Intellectual Property in Health Research & Development; a past member of the European Science Foundation’s Education Working Group, and a past member of the WHO GCP Handbook drafting committee. In addition, he is a member of the Ethics Working Group, European Academy of Paediatrics (UEMS-EAP); and an investigator in several European Commission projects, including ‘The Development of European Standards on Confidentiality and Privacy in Healthcare among Vulnerable Patient Populations’, ‘Ethical Function in Hospital Ethics Committees’, & ‘Ethical Considerations in Clinical Trial Collaboration with Developing Countries’, ‘European Network for Expertise for Rare Paediatric Neurological Disorders (nEUroped)’ and Relating Expectations and Needs to the Participation and Empowerment of Children in Clinical Trials (RESPECT). He is also the past Vice-Chairman of the Ethics Committee of the International Society for Medical Publication Professionals.
He was the Co-facilitator for the Ethics Roundtable at the Africa Centre for Health & Population Studies in South Africa where he also taught a modular GCP course and where he was a member of a DSMB for an HIV vertical transmission study. He is also a member of several regional organizations for ethics in research in Central and Eastern Europe, Asia, Africa, and Latin America. He founded the AfroGuide Project: Developing Guidelines for Health Research in Africa, with the UN Economic Commission for Africa and the African Union. He serves on several editorial boards for international journals.

Maintenance Group
Stage: Completed
Secretariat Liaison: Bridget Walker
TAB Liaison: Anupama Gururaj
Mission The mission of the AIDV-WG is to contribute to building the ethical, legal, social, and technical frameworks for Artificial Intelligence while examining the potential of data visitation to bri...
Working Group
Stage: WG Wrapping up
Secretariat Liaison: Bridget Walker
TAB Liaison: Louise Bezuidenhout
The problem addressed Agricultural data span from field and farm data to scientific and research data to agricultural market data etc. These data are key in fundamental public-good level contexts: foo...
Interest Group
Stage: IG Established
Secretariat Liaison: Bridget Walker
TAB Liaison: Martina Stockhause
Short presentation of Sharing Rewards and Credit (SHARC) IG SHARC is a recognised and endorsed interest group within RDA (Research Data Alliance).  It is an interdisciplinary group seeking to unpack...
Interest Group
Stage: IG Established
Secretariat Liaison: Bridget Walker
TAB Liaison: Mohamed Drira
The proposed activity of this group is to act as a nucleus for discussing requirements for and identifying developments needed to support active (i.e. able to evolve and be monitored) data management ...
Working Group
Stage: WG Wrapping up
Secretariat Liaison: Bridget Walker
TAB Liaison: Mohamed Drira
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Working Group
Stage: WG Wrapping up
Secretariat Liaison: Bridget Walker
TAB Liaison: Niels Deriemaecker
Digital twins, customized simulation models pioneered in industry, are beginning to gain ground in medicine and healthcare, with some major successes in cardiovascular diagnostics and insulin pump con...
Working Group
Stage: WG Producing Deliverables
Secretariat Liaison: Bridget Walker
TAB Liaison: Romain DAVID
This group will develop a standardized Application Programming Interface (API) for machine-actionable Data Management Plans (maDMPs). This API will provide a unified approach to accessing and managing...
Working Group
Stage: WG Wrapping up
Secretariat Liaison: Bridget Walker
TAB Liaison: Martina Stockhause
The Community-based catalogue of requirements for trustworthy Technical Repository Service Providers Working Group (TRSPs WG) will address a significant need in the community of data repositories and ...
Interest Group
Stage: IG Established
Secretariat Liaison: Bridget Walker
TAB Liaison: Curtis Sharma
This Complex Citation Implementation Interest Group is focused on implementing the recommendations developed by the initial Complex Citation Working Group. This interest group includes a broad number ...
Working Group
Stage: Not Yet Endorsed
Secretariat Liaison: Bridget Walker
The Computational Modelling of Health Data working group will focus on improving the reproducibility, transparency, and accessibility of computational models developed for health research. The working...