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Research
Source Data and Case Report Forms
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
Investigational Medicinal Products
Study Samples and Analyses
Adverse Events and Adverse Drug Reactions
Notification of Serious Unexpected Adverse Effects
Reports on Adverse Device Effects
Monitoring and Auditing
Monitoring of the Trial
Notification of the End of the Trial
Reporting of the Study Results
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