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Consulting in preclinical phases (chemistry, pharmacology, toxicology, pharmacokinetics, and pharmacodynamics)

Developing experimental designs and protocols, (including biostatistical analysis), proofs of concept, safety precautions, efficiencies, tolerances, dosages, and monitoring of side effects

Scouting for and selecting potential trial locations

Preparing submission packages and working with the Israeli Ministry of Health and ethics committee at the trial site

Managing data

Managing the trial site, including research and financial contracts, quality agreements, budget management, and -preparation of research documents (staff and patient files, including consent and case report forms and pharmacy files)

Recruiting patients

Providing test-product and storage facilities and continuous monitoring of the supply and trial environment, as well as handling product returns

Monitoring and quality control of clinical trials

Publication writing

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