Provider for clinical research services and education programs in
Israel.
Overview
GCP Clinical Studies Ltd., a leading provider for clinical
Click here to request more information, about this company (FOR COLLABORATION IN R&D. ONLY!)
Note - you have to be registered in this server to
request information. If you haven't done so
yet, please register in this server
Your requests will be forwarded to the developer, who
will contact you directly
You can also see the list of
documents you already requested more information about
research services and education programs in Israel.
The Company is dedicated to assisting the local pharmaceutical
and biotechnology industries to perform their clinical studies,
efficiently, expeditiously and ethically, to create better
health, by bringing new drugs, biologics, and medical devices to
the people who need them.
GCP Clinical Studies Ltd. is divided to Education and Research
divisions:
The Education Division:
GCP Clinical Studies Ltd. has developed collaborative
relationship with the global Association of Clinical Research
Professionals (ACRP) in the area of educational programs for GCP.
Under this collaborating agreement, GCP Clinical Studies Ltd.
delivers exclusively, ACRP's educational programs in Israel. The
educational programs and certification are aimed to all parties
involved in clinical studies including Investigators, Research
Nurses/Coordinators and CRAs (Monitors). GCP's mission statement
is to provide national leadership for the clinical research
profession by promoting and advancing the education and practices
of clinical research in Israel.
The Research Division offers a full range of clinical research
services to both the local pharmaceutical industry and
international companies planning local studies. This includes
Phase 1 - Phase 4 studies as well as post - marketing and drug
surveillance programs.
GCP's goal is to meet your needs by providing a service within
your time and budget limits to ensure rapid market entry.
GCP's service includes:
* Protocol writing and CRF development.
* Feasibility of study in Israel.
* Regulatory and Ethics Committees' Submission.
* Investigators meeting planning and conduct.
* Monitoring; from initiation through site closure visits.
All clinical monitoring activities are performed according to
established ICH guidelines to ensure compliance with GCP.
* Coverage of financial issues; development of clinical trial
agreements, Investigator payments.
* Pharmacovigilance.
* Handling of all drug related issues including distribution.
* Project Management by dedicated study manager;
* Control of monitoring and adherence to monitoring plan
* Regular monitoring meetings to discuss study progress and
recruitment problems.
GCP has significant experience in all the major therapeutic
areas: Cardiovascular, Oncology, Anti-Infective, Antibiotics,
Anti-Virals, Anti retrovirals.
