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NCGS

NCGS, Inc. is a global contract research organization providing a full scope of services needed to successfully plan and conduct all phases of pharmaceutical, biologic, device, and novel diagnostic clinical trials. NCGS has been in operation since 1984 utilizing a customer, site and patient centric approach to study delivery that leverages technology innovation to make timely data-derived decisions. NCGS offers only highly experienced staff with a mean industry tenure of 15 years. Headquartered in Charleston, South Carolina, USA and spanning the US and EU, NCGS has contributed to the approval of 58 products while maintaining a spotless record of zero 483s/regulatory findings in 33 years of operation. NCGS continues to build its reputation with continued focus on integrating high quality technology, staff and processes to provide our Sponsors, sites, and patients with best possible results. NCGS focuses primarily on complex areas of clinical development – oncology-hematology, infectious disease and critical care, CNS (mood, movement, pain and cognition) in both adult and pediatric populations. The universal hope for a cure drives NCGS to deliver high quality results time and again.

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Locations

APAC
Australia
Europe
North America

Overview Accreditations

Therapeutic Areas

Bone / Osteoporosis
Cardiovascular
CNS
Dental and Oral Health
Dermatology
Diabetes
Endocrinology
Gastroenterology
Genetic Diseases
Hematology
Hepatology
Immunology
Infectious Diseases
Inflammation
Internal Diseases
Metabolic Diseases
Musculoskeletal
Nephrology
Neurology
Obstetrics / Gynecology
Oncology
Ophthalmology
Orthopedics
Otolaryngology/ENT (Ear/Nose/Throat)
Pediatrics / Neonatology
Pharmacology / Toxicology
Psychiatry
Pulmonary
Respiratory
Rheumatology
Surgery
Thrombosis
Urology
Vaccines

Accreditations

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 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.