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SGS

SGS Health Science is a leading CRO (contract service organization) offering clinical research and bioanalytical testing with a specific focus on early stage development and biometrics (phase I to IV).

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Locations

APAC
Europe
North America

Overview Accreditations

Therapeutic Areas

Bone / Osteoporosis
Cardiovascular
Central Nervous System (CNS)
Dermatology
Diabetes
Endocrinology
Gastroenterology
Genetic Diseases
Hematology
Hepatology
Immunology
Infectious Diseases
Inflammation
Internal Diseases
Metabolic Diseases
Musculoskeletal
Nephrology
Neurology
Nutrition and Health
Obstetrics / Gynecology
Oncology
Ophthalmology
Orphan/Rare Diseases
Pediatrics / Neonatology
Pharmacology / Toxicology
Psychiatry
Pulmonary
Respiratory
Rheumatology
Special populations like elderly
Thrombosis
Urology
Vaccines
Woman's Health

SGS Health Science is a leading CRO (contract service organization) offering clinical research and bioanalytical testing with a specific focus on early stage development and biometrics (phase I to IV). Delivering solutions in Europe and Americas, SGS offers clinical services encompassing clinical project management and monitoring, medical writing, data management, secure data office, biostatistics, PK/PD data analysis, data visualization, electronic trial master file, medical safety and regulatory.

The SGS biometric group is organized for flexible allocation to meet small, medium and large pharma company’s needs. Our EDC team has extensive experience in customized eCRF build, interactive web response systems and electronic clinical outcome assessment. Through our data visualization services we also offer a wide range of easy-to-understand interactive dashboards that provide complete visibility of your clinical data. SGS is a CDISC registered solution provider and has successfully experienced full electronic submissions for FDA, EMA and PMDA for several candidate drugs. Each service can be provided within full project service outsourcing, a functional service provider (FSP) model or as standalone services.

Documents

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 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.