WHAT WE DO

Vision Statement

Research and Scholarship for an Informed Social Response to Human Life Questions

Mission Statement

The deVeber Institute for Bioethics and Social Research conducts and disseminates research on topics connected to human life in its biological, social and ethical dimensions. These topics are selected for study depending on emerging medical, technological and social developments. In undertaking this work the Institute believes that a sense of the inherent value and dignity of human life and of the human person as an end and not a means is a foundational perspective to bring to bear on its work.

The Institute’s research may be original or may consist of reviews of existing literature. In each case the Institute’s work is to be of the highest academic quality, though accessible to the general public.

MEET US

 Board of Directors

  • Martha Crean — President
  • Robert Parke — Vice-President
  • Patricia Dolente-Matijczyk — Treasurer
  • Ian Gentles
  • Keith Cassidy
  • Dr. Deborah Zeni
  • Dr. Paul Zeni

 Administration

 Advisory Council

  • Dr. Thomas Bouchard
  • Barbara Farlow
  • Lorraine McCallum
  • Dr. David Mikulis
  • Dr. Nancy Olivieri
  • Elizabeth Ring-Cassidy
  • Dr. Jane Pritchard
  • Dr. Paul Ranalli

 Associates

  • Paul Broughton — Publishing Associate

Our History

The deVeber Institute was founded in 1982 and first known as the Human Life Research Institute. A non-profit educational foundation, its mandate was to research and publish studies relating to the impact of biotechnological advances on the individual, family and society, and ethical issues in health care, especially those resulting from reproductive technologies. The Institute remains steadfast to its original vision of an uncompromising commitment to scholarly research. 

The Institute, then and now, is composed of a Board of Directors and an Advisory Council. These men and women come from diverse disciplines including medicine, science, law, social work, history, philosophy, education, business, and journalism. With such depth and range of knowledge, the deVeber Institute takes pride in offering consultation and direction in bioethics. In particular, the media and students have always been encouraged to consult us. 

In 1996, the Board of Directors renamed the organization the deVeber Institute for Bioethics and Social Research. The new name features two key pieces of information, the name “deVeber” and “bioethics and social research.” 

The Board chose to honour Dr L.L. (Barrie) deVeber, then Professor of Paediatrics and Oncology at the University of Western Ontario. Internationally recognized as a pioneer in palliative paediatric care, Dr deVeber had developed a psycho-social team approach to the child with cancer and the family. 

Dr deVeber also directed a program to manage RH haemolytic disease. His team performed the first amniocentesis and intrauterine fetal transfusion in Eastern Canada. Dr deVeber administered the first dose of RH immune globulin in Canada. This treatment eventually eliminated the disease. As a professor, Dr deVeber directed a course in ethics and law for medical students at the University of Western Ontario. 

Because of his experiences in these fields Dr deVeber became aware that there were serious ethical considerations in human life and death issues that were not being adequately and openly addressed. 

The addition of “Bioethics and Social Research” identifies the scope and purpose of the Institute. As reproductive and biomedical technologies continue to affect human life as never before, the Institute addresses key issues with academic integrity and insight. 

For over twenty years the Institute has probed, examined, analyzed, researched and published on topics such as the long-term effects of induced abortion on women’s health and assisted suicide and palliative care. The Institute also conducted original research on unplanned crisis pregnancies and single motherhood in Canada.