CLINICAL TRIALS CENTRE (CTC)
More about CTC
Clinical Trials are an integral and important part of a drug’s life cycle. During their implementation, it is necessary to comply with the legislation of the Czech Republic and the rules of Good Clinical Practice (GCP).
The expert team of the CZECRIN Clinical Trials Unit provides comprehensive and partial services, including consultations and training, for the implementation of academic/non-commercial clinical trials and research in the field of pharmaceuticals, diagnostic methods and medical devices in accordance with the legislation of the Czech Republic and GCP.
LIST OF ACTIVITIES
Study Sponsor Responsibilities and Clinical Trial Project Management
Preparing Clinical Trials Documentation and Application and Medical Writer/Medical Consultant Services
Clinical Trial Regulatory Authority (SÚKL) and Ethics Committee Submission
Data management and biostatistics
Pharmacovigilance
Monitoring
Consulting and Expert’s Advisory
Educational Activities
LIST OF ACTIVITIES
Study Sponsor Responsibilities and Clinical Trial Project Management
Preparing Clinical Trials Documentation and Application and Medical Writer/Medical Consultant Services
Clinical Trial Regulatory Authority (SÚKL) and Ethics Committee Submission
Data management and biostatistics
Pharmacovigilance
Monitoring
Consulting and Expert’s Advisory
Educational Activities
Flyer
Comprehensive summary of information about the Clinical Trials Implementation Unit
CTC Projects
Complete database of projects and studies that have benefited from CZECRIN expertise
Under Construction
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