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Protocol development

At the TCC, we have extensive experience in drawing up protocols for many types of clinical research. Our staff can expand your study outline into a detailed protocol or provide models for you to do this. We can also advise you on how to enhance the quality of a draft protocol, so that it meets all applicable regulations.

We have developed a template to ensure that your protocol includes all relevant information and meets applicable regulations. When writing a protocol or advising investigators, we also refer to the most recent template for a research protocol published by the national regulatory authority of the Netherlands, the Central Committee on Research involving Human Subjects (CCMO).

The TCC employs a team of dedicated methodologists and works closely with professors and faculty staff from the department of epidemiology in the University Medical Center Groningen. This combination enables us to work efficiently, yet also gives you access to the highly specialised methodological knowledge and experience of faculty members if required.