HedrameD is a dedicated independent medical research (out hospital) facility or Site Management Organization (SMO) launched by experienced clinical trial experts in cooperation with forward thinking General Practitioners. We are committed to providing our expertise on clinical trials and site management to the pharmaceutical, biotechnical and nutritional companies and Contract Research Organizations (CRO’s) for the execution of clinical trials. HedrameD is a collaboration of pharmaceutical, medical and managerial experts with a proven track record of nearly 25 years of clinical trials. The HedrameD staff has gained extensive expertise through participation in studies for numerous large pharmaceutical companies, such as Astra Zeneca, PPD, Eli Lilly, MSD, Sanofi-Aventis, Boehringer Ingelheim and others. In Ireland we provide quality services for planning, management and execution of Phase II, Phase III & Phase IV clinical trials including health care/pharmacoeconomic trials in accordance with ICH GCP guidelines. These clinical trials will be reviewed and approved by the Irish Medicines Board, the Medical Ethical Committee and the FDA.