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Turkucrc.fi
Research
Randomisation, Blinding and Coding
Research Plan
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
Monitoring of the Trial
Notification of the End of the Trial
Reporting of the Study Results
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