BRIGHT Research Partners
Bright Research is a clinical research organization (CRO) specializing in medical devices. Founded in 2008 and headquartered in Minneapolis, Minnesota, they manage clinical trials from concept to completion with innovative strategies, superb execution, and personalized service. Their mission is to bring smart research solutions to the medical device community, focusing on innovative strategies, superb execution, and personalized service. They aim to improve the clinical research experience by being kind, honest, and attentive partners to their clients, patients, and employees. Bright Research employs a diverse team of experts including nurses, biomedical engineers, statisticians, PhDs, and seasoned business professionals, trusted advisors on medical device development, clinical study regulations, industry standards, and best practices.
Industries
Nr. of Employees
small (1-50)
BRIGHT Research Partners
Minneapolis, Minnesota, United States, North America
Services
Comprehensive management of clinical studies for medical devices including feasibility, pivotal, and post-market phases.
Support for regulatory interactions and preparation of submission-ready materials for FDA and international regulators, including pre-sub and IDE support.
Statistical design and analysis, sample size planning, and clinical data management to support study outcomes and regulatory submissions.
Design and change management for electronic data capture systems and optimized case report forms to capture required data efficiently.
Identification and qualification of investigator sites, ongoing monitoring, and audit services to ensure protocol compliance and data quality.
Management and execution of post-approval and post-market studies, including literature review and evidence synthesis to inform regulatory and business decisions.
Comprehensive management of clinical studies for medical devices including feasibility, pivotal, and post-market phases.
Support for regulatory interactions and preparation of submission-ready materials for FDA and international regulators, including pre-sub and IDE support.
Statistical design and analysis, sample size planning, and clinical data management to support study outcomes and regulatory submissions.
Design and change management for electronic data capture systems and optimized case report forms to capture required data efficiently.
Identification and qualification of investigator sites, ongoing monitoring, and audit services to ensure protocol compliance and data quality.
Management and execution of post-approval and post-market studies, including literature review and evidence synthesis to inform regulatory and business decisions.
Expertise Areas
- Clinical trial management (medical devices)
- Medical device regulatory strategy and submissions
- Biostatistics and clinical data analysis
- Clinical data management and EDC systems
Key Technologies
- Electronic Data Capture (EDC) systems
- ClinicalTrials.gov registry and reporting
- Biostatistical analysis and study design methods
- Case report form (CRF) design
News & Updates
Bright Research participated in LSI 2025, a major event in the industry.
Bright participated in the MDIC Case for Quality Collaborative Community Workshop in Medical Alley.
Bright team attended the International Stroke Conference 2023.
Bright team attended the CRT2024 conference.
Bright team attended the MedTech MVP 2024 conference.
A review of Bright Research's achievements and activities in 2024.
Bright Research participated in LSI 2025, a major event in the industry.
Bright participated in the MDIC Case for Quality Collaborative Community Workshop in Medical Alley.
Bright team attended the International Stroke Conference 2023.
Bright team attended the CRT2024 conference.
Bright team attended the MedTech MVP 2024 conference.
A review of Bright Research's achievements and activities in 2024.