Can someone describe the commercialization process in Israel? Assuming we have all of the clinical data necessary, what are the steps with the Israeli Ministry of Health? How many face-to-face meetings are required, ie, are there Quality and Clinical consultations like with PMDA? What is the application fee? Does all of the material need to be translated and if so, is it common to lean on an Israeli consultant vs CRO to do this? Thank you!
------------------------------
Candace Hsieh
Irvine CA
United States
------------------------------