Clinical Trial National Centre
Expertise and services
Comprehensive expert support of clinical research from study design to the use of results in practice.
Expertise and services
CZECRIN provides comprehensive expert support throughout the entire clinical trial lifecycle – from initial design through the approval process to implementation, data analysis and strategic use of results.
Individual services are grouped by study phase and type of expertise to make it easy to find the right support at the right time.
Preparation and conduct of a clinical trial
When to contact us
When you have a research idea, grant project or clinical question
and need to translate it into a feasible study.
Commissioning and project management of the study
Preparation of study documentation
medical writer and consultant
consulting and advisory activities
Regulation, ethics and compliance
When to contact us
When you need to safely go through the approval processes and navigate the regulatory requirements in the Czech Republic and the EU.
Processing the study with the regulatory authority
Processing of the study by the ethics committee
Implementation and supervision of the study
When to contact us
During the active phase of a clinical trial, when it is crucial to ensure data quality, patient safety and protocol compliance.
MOnitoring
pharmacovigilance
Data, statistics and scientific support
When to contact us
When you need expert support in data handling, analysis and interpretation in accordance with scientific and regulatory standards.
Statistics
Methodology, training and capacity development
When to contact us
If you want to strengthen your competence in clinical research, methodology and quality in the long term.
Strategic and specialised services
When to contact us
In cases requiring superior expertise, international coordination or strategic decision-making in clinical research and healthcare.