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Worldwide Clinical Trials

A full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications. Capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies.

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Locations

APAC
Australia
Europe
North America

Overview Accreditations / Enablement

Therapeutic Areas

Cardiovascular
CNS
Dermatology
Diabetes
Endocrinology
Genetic Diseases
Hematology
Immunology
Infectious Diseases
Inflammation
Internal Diseases
Metabolic Diseases
Musculoskeletal
Neurology
Oncology
Ophthalmology
Orthopedics
Otolaryngology/ENT (Ear/Nose/Throat)
Pediatrics / Neonatology
Pharmacology / Toxicology
Psychiatry
Pulmonary
Rare Disease
Respiratory
Rheumatology
Sleep
Surgery
Vaccines

Worldwide Clinical Trials (Worldwide) is a full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications.

Worldwide’s capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by an accessible team of clinicians, scientists, and researchers who bring first-hand expertise and a collaborative, personalized approach to each clinical program.

Worldwide is therapeutically focused on neuroscience, oncology, rare disease, and cardiometabolic and inflammatory disease. Its global footprint spans over 60 countries with more than 3,500 team members. For more information, visit www.worldwide.com.

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 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 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.