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

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.
Endpoint experience of working across a large number of companies from the smallest start-up ventures, through Biotech and Medical Device companies to large CROs and drug companies. Since established, Endpoint successfully completed over 30 local and international projects, employ 3 full time CRA and 2 CTA. Managed by Ilana Fishman (M.Sc.), Senior CRA II an appreciated professional with more than two decades of combined industry experience, Endpoint maximizes the benefits of the region with a complete understanding of international research standards.

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

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.
Our team of dedicated research and clinical professionals has worked to develop strong relationships with each sponsor, client and clinical sites, based on mutual respect and a scientific understanding among peers.

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

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.
Although Endpoint offers the full range of study services we can offer this support in a modular way, depending on the client's needs, integrating smoothly into our client's project teams.

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

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.
We are dedicated to client support and take full responsibility for achieving extraordinary results by providing critical thinking, better insights, and timely responsiveness. We are able to be flexible and focus on tailoring projects, as per clients and projects needs and requirements.
We are following client's timelines and project milestones, data base submission deadlines.

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

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.
Endpoint personnel is fully certified for working with Global pharmaceutical companies, such as Novartis Pharma Services and Pfizer, as well as Medical Devices companies, such as ConorMed Systems (J&J) and Given Imaging.