「創薬ボランティアのしおり」,「被験者管理票」の利用と治験コーディネーター業務

概要

論文の詳細を見る
Recently, pharmacists are playing actively roles in coordinating clinical trials under the protocol of each investigational new drug and also play an important role in the total management of clinical trials. Since April 1999, we initiated several new clinical research coordinator (CRC) services, such as, support for obtaining informed consent, the schedule setup of studies, follow-up of involved patients, monitoring and audit of studies and collaboration in writing case report forms. As one of new trials we have developed in CRC services Is a Personal Booklet of volunteers for clinical trials to inform the patients about the clinical trials and to also facilitate the communication between the patients and CRC. In addition, we made a Subject Data Profile to share all information concerning clinical studies among CRC s. We believe that such trials may help to greatly improve the quality of such CRC services.
日本医療薬学会の論文
2000-10-10