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Clinical Trials

At BioForum we see clinical trials as the heart of any pharmaceutical or medical device company. As part of this philosophy, we have chosen to bring our clinical trial services and training programs to the forefront of our operations. We are proud to offer the following services:

Orit Booganim,
Business & Development Manager

Mobile: +972-52-5904499
Tel: +972-3-9244410
Fax: +972-3-9244420
E-mail: orit_b@qt.co.il

Clinical Trial Training Programs: (click here for all courses)
CRA training
The management of the entire clinical trial process, from the selection of medical centers and investigators to closure of sites and documents, including adhering to GCP requirements and local regulation regarding participants' rights are the responsibility of the Clinical Research Associate – the “Monitor”. This course provides more than just the basics of clinical trial management and qualifies participants as Clinical Research Associates.
CRC training
Clinical Research Coordinators, the professional liaison between sponsor and Ethics Committee, investigator and medical professionals, and medical staff and laboratory, bear the responsibility for locating and recruiting subjects for clinical trials and overseeing all aspects of the trial. This course gives comprehensive training for participants, covering regulatory demands of the FDA, the EU and Israeli authorities, informed consent, GCP, medical ethics, and more.
GCP training
Good Clinical Practice, a term which relates to ethics and regulatory demands in clinical trials, is the basic underlying guidelines for all clinical trial professionals. This course covers ICH-GCP regulations, medical ethics, protocol, investigational product, and other aspects of clinical trials necessary for success in compliance with GCP requirements.

Pre-Clinical Trial Training Programs (click here for all courses)

GLP
Courses offering participants skills for conducting pre-clinical stage trials, including regulations, planning and implementation, documentation, and animal treatment.

 


BioForum offers a complete Clinical Data Management Consulting Services for Clinical Trials for Parmaceutical and Medical Device Development.
for more information please click here


Bioforum offers senior professionals in clinical trials assistance in writing, editing and translating of all documents needed for clinical trials.
Our experts provide a combination of academic knowledge and professional writing skills, which is a guarantee for high quality and cost effectiveness.
for more information please click here

Experts' Center

Useful Links
For links please click here

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