Find A Partner CTI Clinical Trial and Consulting Services

CTI Clinical Trial and Consulting Services

CTI Clinical Trial and Consulting Services is a global, privately held, research service organization, delivering a complete spectrum of clinical trial and consulting services throughout the lifecycle of development, from concept to commercialization. CTI’s focused therapeutic approach provides pharmaceutical, biotechnology, and medical device firms with clinical and disease area expertise in rare disease, regenerative medicine / gene therapy, immunology, transplantation, nephrology, hematology / oncology, neurology, infectious disease, hepatology, cardiopulmonary, and pediatric populations. CTI also offers a fully integrated multi-specialty clinical research site, complete global laboratory services, and contract development and manufacturing services. Now in its third decade, CTI is one of the 20 largest contract research organizations (CROs) in the world, with associates in more than 60 countries across six continents. CTI is headquartered in the Greater Cincinnati area, with operations across North America, Europe, Latin America, Middle East and Africa, and Asia-Pacific. For more information, visit www.ctifacts.com and follow us @cticlinicaltrials.

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Locations

Africa
APAC
Australia
Europe
North America
South America

Overview Accreditations / Enablement

Therapeutic Areas

Cardiovascular
CNS
Dermatology
Diabetes
Endocrinology
Gastroenterology
Genetic Diseases
Hematology
Hepatology
Immunology
Infectious Diseases
Inflammation
Metabolic Diseases
Musculoskeletal
Nephrology
Neurology
Obstetrics / Gynecology
Oncology
Ophthalmology
Other
Pediatrics / Neonatology
Pharmacology / Toxicology
Pulmonary
Respiratory
Rheumatology
Sleep
Surgery
Thrombosis
Vaccines

Accreditations / Enablement

Partners are trained on the functionality of the Coder application, process optimization, and scope of Coder services. This Accreditation teaches Partners to integrate the medical coding solution with EDC studies and administer Coder segments. Coder Accreditation is dependent on the successful completion of the Rave EDC accreditation.

Partners are trained on the functionality of the eCOA application, best practices, process optimization and the scope of eCOA services. This Accreditation teaches Partners to process patient data that has been entered by the patient themselves, or by a Clinician. Patients enter their patient data through a provisioned device or their own device after downloading the appropriate app. Clinicians enter patient data through a provisioned device (Android or iOS). eCOA Accreditation is dependent on the successful completion of the Rave EDC Accreditation.

Partners are trained on the functionality of the electronic data capture (EDC) and clinical data management (CDM) system, process optimization exercises and scope of Medidata Rave services. This Accreditation teaches the staff to perform end user training, user and site administration, study build, reporting, outputs and amendment manager.

Partners are trained on the functionality of the RTSM Application, process optimization, best practices using RTSM, and scope of RTSM services. This Accreditation teaches Partners to conduct randomization and clinical trial supply management services (RTSM). RTSM Accreditation is dependent on the successful completion of the Rave EDC Accreditation.

Partners are trained on the functionality of the Safety Gateway application, process optimization, and scope of Safety Gateway services. This Accreditation teaches Partners to utilize the configurable EDC-to-safety-system interface to automate advanced serious adverse event (SAE) collection and E2B transmissions. Safety Gateway Accreditation is dependent on the successful completion of the Rave EDC Accreditation.

Partners are trained on the functionality of the targeted source document verification (TSDV) application, process optimization, and scope of TSDV services. This Accreditation teaches Partners to implement TSDV in line with regulatory compliance and data quality strategies. TSDV Accreditation is dependent on the successful completion of the Rave EDC Accreditation.

Partners are trained on the functionality of the Medidata Remote Source Review application, best practices and scope of Medidata Remote Source Review services. The Accreditation will focus on support source document collection, uploaded document quality control and site query(ies). This Accreditation teaches the Partners to perform configuration of studies, end user training, and user and site administration for Remote Source Review studies.