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Clinical Research |
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Clinical Research is conducted according to guidelines of the Ministry of Health, and in accordance with GCP-ICH regulations.
All protocols must be approved by the Institutional Review Board (IRB) - Ethics Committee.
We have ongoing research contracts with major international pharmaceutical companies and CROs, as well as with Israeli biotechnology companies. TASMC has an in-house phase I Clinical Trial Center,
as well as services to expedite clinical trials - CTNS.
Researchers and representatives of pharmaceutical, biotechnological and medical device companies interested in promoting clinical trials inthe framework of the Medical Center are invited to approach the Division of R & D - Galya - clintrials@tasmc.health.gov.il for assistance, forms and guidance. We have standard contracts with commercial organizations and recommend that company representatives meet with us to finalize agreements, so when protocols are approved by the IRB, permission to begin the trials can be given. |
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