Site Management Organization


All personnel involved in the clinical trial must be qualified by training. Training offered are Good Clinical Practice (GCP), Protocol Development, Manuscript writing, and Study Coordinator Training. Prodia CRO may help you in organizing and providing these trainings for all study personnel before the start of the clinical trials.

Good Clinical Practice (GCP) Training


Every implementation of clinical trials in Indonesia should be carried out in accordance with good clinical practice (GCP) guidelines. One of the GCP requirement for investigator and the study team is to have qualifications and competencies to perform the trial according to GCP. To support this, PT Prodia Diacro Laboratories in collaboration with The Indonesian Association for the Study of Medicinals (IASMED) provide in-house Training Course & Workshop on Applied Good Clinical Practice. In these sessions, participants will be trained by the experts in the field of clinical trials.

This will benefit the trainee in preparing, implementing, and evaluating the implementation of a clinical trial. During the workshop sessions, participants will be involved in an interactive session in stimulating the application of GCP principles in day-to-day clinical trial implementation. At the end of the course, the participants will sit to join the final test of the GCP Course to be able to obtain certificate of competency.

Would you like to know more about Site Management Organization Services?

Would you like to know more about our Site Management Organization Services?