Orizzonte Clinical Research

Orizzonte Clinical Research is listed as a new startup research supplier in the Scientist.com network, with 1 site in 1 country.

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Search companies, drugs, suppliers and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.

Sites 1

Countries 1

Type of company: New startup

Clinical Protocol Design & Development Creation of clinical protocol document which details how a clinical trial is designed, relating to to the methodology, hypothesis, and operation of clinical trial to ensure the safety of the patients is...

Clinical Trial Design Develop study-related protocols, case report forms (CRFs) and database tools for records management.
eConsent - Electronic Informed Consent Monitor clinical trials through electronic informed consent given by patients.
IP Import/ Export Licensing Receive assistance with intellectual property import and export licensing.
Patient Recruitment Recruit and retain patients for clinical trials.
Phase 1-3 Studies Design phase 1-3 studies that seek to identify if a drug is safe, effective, and more efficient than other available treatments on the market.
Post-Marketing (Phase 4) Studies Conduct phase 4 studies for confirming unrecognized safety issues, investigating possible hazards or establishing the expected safety profile of a veterinary medicinal product under market conditions.

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Site Monitoring Maintain oversight over participant's health during a clinical trial.
Site Selection Select clinical trial sites with clinicians who recruit, enroll, treat and evaluate trial patients.
Study/Site Feasibility Study Explore and test study practicality.

Communication Plan Communications plan enables organizations and corporations to effectively deliver information to appropriate stakeholders and customers.

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