Premium Israeli CRO

Delivering Quality Since 2005
Endpoint is a full service premium contract research organization (CRO), experienced in performing clinical development activities in pharmaceutical and medical devices studies in Israel. Endpoint has been performing clinical research in this growing and dynamic region of the world since 2005. Read more

Experienced Team Members
Endpoint maintains a staff of experienced professionals in the area of clinical research. Our CRAs all have medical or biological degrees with at least of 3 years of industry experience. Read more

Regulatory and Logistical Support
Endpoint has developed internal processes to expedite the regulatory process, provide logistical oversight for international shipments, and establish regulations that incorporate good clinical practices. The end result is a project management driven organization focused on the needs of our global clients and the regulatory authorities we each need to satisfy. Read more

We have you covered from start to finish
Endpoint will handle all sites feasibility and evaluation, submission to IRBs, conduct and of course closure for your trial from beginning to the end. Endpoint will carefully and completely walk you through the study planning, building of essential documents via submission and study conduct procedures to the final study report. Let our local experience be your international strength. Read more

Regional Focus with Global Perspective
Since established, Endpoint provided full CRO and regulatory services to large number of local start up biotechnology and medical devices companies, required full compliance with FDA, local and International regulations. Read more

Ilana Fishman Dembo
CEO, Senior Clinical Research
Associate II
M +972 54 7545065
T +972 77 2345829
F +972 77 2345828