CLINICAL TRIAL CENTRE (CTC)

About CTC

Clinical Trials are an integral and essential part of the drug life cycle. During their implementation, it is necessary to comply with the Czech Republic’s legislation and the rules of “Good Clinical Practice (GCP).

CZECRIN Clinical Trial Centre expert team provides comprehensive and partial services, including consultations and training, to implement academic/non-commercial clinical trials and research in the field of medicinal products, diagnostic methods and medical devices following Czech and GCP legislation.

CTC 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 a biostatistics

Pharmacovigilance

Monitoring

Consulting and Expert's Advisory

Educational Activities

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CTC Summary Information

Under Construction

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CTC Projects

Complete database of projects and studies that used CZECRIN expertise.

Under Construction

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