New guidelines & documents
- En ny biobankslag - lagrådsremiss (April 2022)
- Clinical Trials Regulation EU No. 536/2014
- Registering your clinical study (Swedish Research Council, 2022)
- General considerations for clinical studies (ICH)
- Guidelines 05/2021 on the Interplay between the application of Article 3 and the provisions on international transfers as per Chapter V of the GDPR
- ICMJE Disclosure of Interest form
- Guidelines for Tailoring the Informed Consent Process in Clinical Studies (I-Consent)
- Recommendations for the handling of ethical concerns relating to the publication of research data (Force 11 & COPE)
- The Tianjin Biosecurity Guidelines for Codes of Conduct for Scientists
- STM Recommendations for handling image integrity issues
- Should I include studies from “predatory” journals in a systematic review? Interim guidance for systematic reviewers (article)
- Clinical research in resource-limited settings (CIOMS)
- WPA Code of ethics for psychiatry
- Reflecting Sunlight. Recommendations for Solar Geoengineering Research and Research Governance (National Academies, US, 2021)
- Ethical considerations in HIV prevention trials (updated) (UNAIDS/WHO)
Earlier documents (in alphabetical order):
- Act on responsibility for good research practice and the examination of research misconduct, SFS 2019:504 (Ministry of Education and Research)
- Addressing ethical dilemmas in AI: Listening to the engineers
- AMWA–EMWA–ISMPP joint position statement on predatory publishing
- A Preliminary Opinion on data protection and scientific research (The European Data Protection Supervisor)
- Beijing Declaration on Research Data (International Science Council)
- Ethical licences (The ethical source movement)
- Etikprövning av forskning – tydligare regler och skärpta straff - Prop. 2018/19:165 (Ministry of Education and research)
- Etiska aspekter i samband med utlandsstudier (Lunds etikråd)
- Förordning om ändring i högskoleförordningen (1993:100)
- Good Practice for Conference Abstracts and Presentations: GPCAP (article)
- Informed Consent Standard for Stem Cell-Based Interventions Offered Outside of Formal Clinical Trials
- Model consent clauses for rare disease research (BMC article)
- Ny ordning för att främja god sed och hantera oredlighet i forskning, prop. 2018/19:58
- Personuppgiftsbehandling vid antalsberäkning inför klinisk forskning (SOU 2020:53)
- Recommendations for the Investigation of Research Misconduct (ENRIO)
- TOP Guidelines (Center for Open Science)
- Transparency Checklist for Social & Behavioural Research
- Vägledning för hanteringen av misstankar om avvikelser från god forskningssed (SUHF)

Last modified: 2022-04-18