EXPERTISE
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
