Become a partner

informerat samtycke

informed consent [ENGLISH]

Documented voluntary agreement made by a person, or their legal representative, to participate in a clinical study, after they have been informed of the study’s nature, procedure, importance, implications, possible risks and benefits, alternatives and the person’s right to withdraw from the study.

informerat samtycke [SWEDISH]

Ett godtagande till att medverka som grundar sig på tydlig och utförlig information vad ett deltagande (i en klinisk studie) innebär.


Resources and references

Definitions have been translated into the Swedish language from the following sources:

  1. 1. American Society of Gene and Cell Therapy Glossary
  2. 2. Clinical Trials Information System
  3. 3. EMA Glossary of Regulatory Terms
  4. 4. EMA Medical Terms simplifier
  5. 5. Glossary of Terms used in EU Clinical Trials Register
  6. 6. Glossary of Terms U.S Food and Drug Administration
  7. 7. National Human Genome Research Institute “Talking Glossary of Genomic and Genetic Terms”
  8. 8. The Glossary for Advanced Therapies Regen. Med. Dec 2020 Vol. 15 No. 12 Suppl. 1
  9. 9. Toolkit For Patient Focused Therapy Development Glossary

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