Clinical Trial Services


GCP Training

At CCA we offer comprehensive ICH GCP training. Understanding the value and importance of ICH GCP and its implementation within a clinical trial and biopharmaceutical setting is vital to the continued safety of clinical patients, which above all things is what clinical ethics holds as its highest benchmark. Understanding and valuing these ideals promotes more diligent monitoring practices such as source document verification, strict compliance requirements, drug accountability and ultimately the veracity of the data that is collected from the different stages of clinical trials.


Our course gives an up-to-date and comprehensive guide to the basic principles of ICH Good Clinical Practice and covers all the new changes/amendments proposed in the EU Directive 2005/28/EC. As prescribed by the international standards and requirements, a basic understanding of Good Clinical Practice is pre-requisite for anyone carrying out, or involved with, clinical research and clinical trials. The training is therefore crucial for:

  • Investigators from NHS/ HSE organisations, university hospitals, pharmaceutical companies and research institutes
  • Research Nurses
  • R&D staff involved with approving and monitoring clinical trials
  • Members of ethics committees
  • Clinical trials support staff