The Patients Network for Medical Research and Health is working for a voice in research and health policy and seeks a world in which genetic diseases are understood, effectively treated, prevented and the people affected supported.
EGAN’s position and policies on current issues in genetics and health care delivery: diagnosis, testing, screening, stem cells, reproductive choice, gene, cell and tissue therapy, paediatric medicines, biobanks, patenting and intellectual property and animal experimentation. The Patients Network for Medical Research and Health welcomes collaboration with all organisations, institutions and societies which can contribute to achieving its goals.
EGAN voices and articulates a clear, patient focussed perspective on genetic and medical biotechnological issues and their ethical, legal, psycho social and cultural implications in the European political, scientific and industrial arena.
Contact and further information
EGAN Secretariat
Koninginnelaan 23
3762 DA Soest
The Netherlands
P. + 31 35 6034040
F. + 31 35 6027440
E. egan@egan.eu,
VSOP Koninginnelaan 23
3762 DA Soest
T +31 35 6034040
F +31 35 6027440
vsop@vsop.nl
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