Glossary Term
Volunteer Registry
Definition
A volunteer registry is a database or platform that collects and maintains information about individuals who have expressed interest in participating in clinical trials, research studies, or volunteer programs. These registries help connect volunteers with relevant studies, facilitating participant recruitment. The registry may include demographic details, medical histories, and other relevant information to match potential participants with studies that align with their characteristics and health profiles. A volunteer registry can be an important tool for researchers and clinical trial sponsors to quickly find eligible participants, streamline recruitment, and ensure diverse and representative samples for studies.
Relevance to the MedTech Industry
Volunteer registry efficiently manage and organize potential participants for clinical trials, research studies, or medical device testing. By maintaining a comprehensive list of volunteers, research teams can easily access and contact individuals who meet the criteria for participation, ensuring that studies are conducted in a timely and effective manner. Registries also improve patient recruitment by increasing awareness and accessibility for volunteers interested in participating in clinical research.
Additional Information & Related Terms
Related Terms
Clinical Trial Recruitment: The process of identifying, contacting, and enrolling participants for clinical trials, often facilitated by volunteer registries.
Informed Consent (eConsent): The process of ensuring that participants understand the risks and benefits of participation in a clinical trial, which is a key aspect of volunteer registry operations.
Patient Registry: A database of patients who have volunteered to provide ongoing data for research, which may serve as a source for clinical trial recruitment.
Recruitment Strategies: Techniques used to increase enrollment and engagement in clinical trials, such as using volunteer registries, social media, or direct outreach.
Real-World Evidence (RWE): Data collected from real-world settings, such as post-market studies, where volunteer registries may be used to track patient outcomes or product performance.