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)