Siara

International Conference of Harmonisation of the Technical Requirements for the Registration of Pharmaceuticals for Human use (ICH) Good Clinical Practice (GCP) Guidelines (E6) and related guidelines. Siara offers unparalleled training programmes and consultancy to: Clinical Research Professionals in the Pharmaceutical, Biotechnology and CRO industry. Clinical Investigators and Site Staff Independent Ethics Committees Siara specializes in: Educating and training clinical research professionals on the requirements of internationally recognised standards when conducting clinical research in human subjects from protocol design, through to study conduct and final study report writing. Providing guidance and consultancy on the ethical principles to physicians and clinical research professionals in medical research involving human subjects. Nurturing of Investigative sites into ‘Centres of Excellence’ for clinical research and hence building capacity for the conduct of good clinical research.