RD-ConnectRD-Connect

  • About
    • Introduction to rare diseases
    • Structure
      • Executive Management Committee (EMC)
      • Scientific Advisory Board (SAB)
      • Patient Advisory Council (PAC)
      • Rare Disease Patient and Ethics Council (RD-PEC)
      • Panel for Biobank Assessment
    • Collaborations
  • What we do
    • Data linkage
      • FAIRification of rare disease registries
      • Linked data and ontology task force
      • Ontologies in rare disease registries
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    • Phenotypic data
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      • Core Implementation Group
    • Biosamples data
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      • Sample Catalogue
      • Biobank assessment process
      • Biobank Assessment Panel
    • Bioinformatic tools
    • Ethical, Legal and Social Issues (ELSI)
      • Sharing of biosamples and data
      • Standards for informed consent
      • Response to the EU General Data Protection Regulation (GDPR)
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    • Periodic activity reports
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Simon Woods

RD-Connect

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Simon Woods

Position: Senior Lecturer and Co-Director PEALS
Organisation: Newcastle University
Area of work: Ethical Legal Social Issues

Member of: The Rare Disease Patient and Ethics Council (RD-PEC)

Contact information:

Email

Role in RD-Connect:

Simon Woods is a member of the Rare Disease Patient and Ethics Council (RD-PEC).

Background:

Simon Woods is Senior Lecturer and Co-Director of the Policy Ethics and Life sciences Research Institute (PEALS) at Newcastle University (an interdisciplinary bioethics research centre). Simon has a longstanding interest in the ethics of research; he is vice-chair of an research ethics committee at the British National Health Service (NHS) and is a member of the National Research Ethics Service National Ethics Advisors’ Panel. In addition Simon has been active as an Ethical, Legal and Social Implications (ELSI) work-package leader, or ethics advisor to several EU projects with a focus on rare disease genomics (DGEMap, TREAT-NMD, BIO-NMD, NMD-Chip, RD-Connect). Simon holds doctoral degree in philosophy and over the past 10 years he has pursued a career of teaching and research within bioethics. Simon has considerable expertise in the ethics and regulation of bioscience research.

Visit the platform

Go to Genome-Phenome Analysis Platform

Go to Registry & Biobank Finder

Go to Sample Catalogue

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Recent news

RD-Connect Genome-Phenome Analysis Platform is an IRDiRC Recommended Resource

Published: April 5, 2018

RD-Connect in press

Published: March 1, 2018

Today is the Rare Disease Day 2018

Published: February 28, 2018

Key RD-Connect, NeurOmics and EURenOmics publication

Published: February 27, 2018

RD-Connect and EURenOmics among the DG Research success stories

Published: February 15, 2018

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An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research. Visit the platform:

Genome-Phenome Analysis Platform

Analyse and share genomic data

Registry & Biobank Finder

Directory of rare disease biobanks and patient registries

Sample Catalogue

Browse rare disease biosamples stored in biobanks

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  • NEWS
  • EVENTS
  • CONTACT
    • Coordination office
    • Contacts Directory
    • Organisations Directory
  • About
    • Introduction to rare diseases
    • Structure
      • Executive Management Committee (EMC)
      • Scientific Advisory Board (SAB)
      • Patient Advisory Council (PAC)
      • Rare Disease Patient and Ethics Council (RD-PEC)
      • Panel for Biobank Assessment
    • Collaborations
  • What we do
    • Data linkage
      • FAIRification of rare disease registries
      • Linked data and ontology task force
      • Ontologies in rare disease registries
    • Omics data
      • Genome-Phenome Analysis Platform
    • Phenotypic data
      • Registry & Biobank Finder for patient registries
      • Registry common data elements
      • Core Implementation Group
    • Biosamples data
      • Registry & Biobank Finder for biobanks
      • Sample Catalogue
      • Biobank assessment process
      • Biobank Assessment Panel
    • Bioinformatic tools
    • Ethical, Legal and Social Issues (ELSI)
      • Sharing of biosamples and data
      • Standards for informed consent
      • Response to the EU General Data Protection Regulation (GDPR)
    • Patient engagement
  • Resources
    • Newsletters
    • Scientific publications
    • Forms and guides
    • Presentations and flyers
    • Periodic activity reports
    • Glossary
  • For Patients and Families
  • News
  • Events
  • Contact
    • Coordination office
    • Contacts Directory
    • Organisations Directory

Quick links

  • Genome-Phenome Analysis Platform
  • Registry & Biobank Finder
  • Sample Catalogue

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RD-Connect

RD-Connect coordination team
Institute of Genetic Medicine
University of Newcastle upon Tyne
International Centre for Life
Newcastle upon Tyne
NE1 3BZ
United Kingdom

Email: Libby Wood (Project Manager)

T: +44 191 241 8621
F: +44 191 241 8770

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