fi
Our Services
Counselling Services at TurkuCRC
Services for the Sponsor
Permissions and Guidance
Ethics Committee Review
Permissions for Clinical Trials
Trial Agreements and Insurance
Clinical Trial Registration
Links to Useful Forms and Templates
Policies and Guidance for Health Related Research
Links to Legislation, Policies and Guidelines
Research
Research Plan
Subject Recruiting
Informed Consent
Informed Consent Document
Compensation to Study Subjects in Clinical Research
Subject Screening
Randomisation, Blinding and Coding
Investigator's Brochure
Investigator's Trial File
Source Data and Case Report Forms
Study Samples and Analyses
Monitoring and Auditing
Notification of the End of the Trial
Reporting of the Study Results
Archiving
Courses
Centre for Clinical Informatics
Innovations
Contact
fi
Turkucrc.fi
Permissions and Guidance
Ethics Committee Review
Permissions for Clinical Trials
Permission for Medical Trials
Permissions for Clinical Trials on Medicinal Products
Permission for Registry Studies
Permission for Biological Sample Studies
Permission for Nursing Science Studies
Permission for Medical Devices Trials
Notification to Valvira
Permission for Biobank Studies
Trial Agreements and Insurance
Financing
Trial Agreements
Insurence Policies for Study Subjects
Clinical Trial Registration
Links to Useful Forms and Templates
Policies and Guidance for Health Related Research
Medical Research Act
Researcher
Commissioning Party
Act on the Openness of Government Activities
Principles of the Clinical Research Ethics
Responsible Conduct of Research
The Princeples of Good Clinical Practice
General Data Protection Regulation in EU
Disclosure of Interests
Open Science and Research
Digital Identifier for the Researcher
Evaluation of the Effectiveness of the Research
Links to Legislation, Policies and Guidelines
Back to top
