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PROMETRIKA, LLC

PROMETRIKA, LLC is a global clinical research organization (CRO) expertly supporting the biopharmaceutical and medical device industries since 2003. Based in Cambridge, Massachusetts, a biopharmaceutical hub, PROMETRIKA has provided over 20 years of experienced, professional support to local, national, and international clients. We enjoy strong, collaborative relationships with companies developing some of the most innovative and promising new therapies. We deploy a collaborative approach to clinical development and execution with a close-knit, highly experienced senior leadership team who remain involved throughout the duration of each trial. Our team has successfully delivered hundreds of clinical studies, phase 1 through 4, in drugs, medical devices, biologics, and diagnostics across all major therapeutic areas. We offer full services in clinical operations, data management, biostatistics and programming, medical writing, drug safety management, and regulatory submissions.

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Locations

Africa
APAC
Australia
Europe
North America
South America

Overview Accreditations

Therapeutic Areas

Allergy
Cardiovascular
Dermatology
Diagnosis & Imaging
Endocrinology
Gastroenterology
Hematology
Immunology
Infectious Diseases
Inflammation
Medical Device
Nephrology
Neurology
Oncology
Ophthalmology
Orthopedics
Pain Medicine
Pediatrics / Neonatology
Psychiatry
Pulmonary
Rare Diseases
Rheumatology
Urology
Woman's Health

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.