The Short Consent Form For Research is a crucial document used in Austrian research settings to obtain legally valid informed consent from study participants. This document is essential when conducting any research involving human subjects in Austria, whether in academic, medical, or commercial settings. It must comply with the EU General Data Protection Regulation (GDPR), Austrian Data Protection Act (DSG), and relevant research ethics guidelines. The form serves as a legal record of participant consent while ensuring transparency about research procedures, risks, and data handling. It should be used at the initial stage of participant recruitment and must be obtained before any research procedures begin. The document is designed to be accessible to lay persons while maintaining legal validity under Austrian jurisdiction.
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1. Title and Introduction: Clear identification of the research study and institution
2. Researcher Information: Names and contact details of principal investigators and research team
3. Purpose of the Study: Clear, non-technical explanation of research objectives and importance
4. Study Procedures: What participation involves, including time commitment and activities
5. Risks and Discomforts: Potential risks, side effects, or inconveniences
6. Benefits: Direct and indirect benefits of participation
7. Data Protection and Confidentiality: How personal data will be collected, stored, and protected (GDPR compliance)
8. Participant Rights: Right to withdraw, access data, and file complaints
9. Costs and Compensation: Any payments, reimbursements, or costs involved
10. Declaration of Consent: Clear statement of voluntary participation and signature section
1. Future Research Use: Include when data/samples might be used in future studies
2. Commercial Development: Include when research might lead to commercial products
3. Genetic Testing Information: Include for studies involving genetic analysis
4. Photography/Video Recording: Include when research involves media recording
5. Covid-19 Precautions: Include for in-person research during pandemic conditions
6. Third Party Data Sharing: Include when data will be shared with other institutions
7. Translation Statement: Include when form is provided in multiple languages
1. Detailed Study Protocol: Technical description of research methodology
2. Data Processing Agreement: Detailed GDPR-compliant data handling procedures
3. Contact Information Sheet: Complete list of research team and emergency contacts
4. Withdrawal Form: Template for participants to withdraw from the study
5. Glossary: Definitions of technical terms used in the consent form
6. Rights Summary: Detailed explanation of participant rights under GDPR and Austrian law
Relevant legal definitions
Clauses
Relevant Industries
Healthcare
Pharmaceutical
Biotechnology
Academic Research
Clinical Trials
Medical Devices
Psychology
Social Sciences
Market Research
Educational Research
Public Health
Relevant Teams
Legal
Research & Development
Clinical Operations
Regulatory Affairs
Ethics Committee
Data Protection
Research Administration
Clinical Trials
Human Resources
Quality Assurance
Research Compliance
Medical Affairs
Relevant Roles
Research Director
Principal Investigator
Clinical Research Coordinator
Ethics Committee Member
Data Protection Officer
Research Ethics Officer
Legal Counsel
Research Administrator
Clinical Trial Manager
Research Compliance Officer
Research Nurse
Study Coordinator
Research Project Manager
Institutional Review Board Member
Research Department Head
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