Medrio
Medrio provides a comprehensive suite of clinical trial solutions, including CDMS/EDC, eCOA/ePRO, eConsent, RTSM, Clinical Data Services, and Clinical Trial Project Management, all while ensuring compliance with major regulatory standards.
Medrio Services
Medrio offers a comprehensive suite of clinical trial solutions designed to support various aspects of clinical research. Their services include Clinical Data Management Systems (CDMS) and Electronic Data Capture (EDC) software, which provide robust data capture and management capabilities. Additionally, Medrio offers electronic patient-reported outcomes (ePRO) and electronic clinical outcome assessments (eCOA) solutions. Their eConsent platform aims to streamline the informed consent process, enhancing both compliance and participant experiences. The Randomization and Trial Supply Management (RTSM) service is designed to optimize study supply management and eliminate bias in clinical trials. Medrio also provides Clinical Data Services to support project data management needs and Clinical Trial Project Management services to ensure strategic and efficient project execution.
Medrio Products
Medrio delivers a range of specialized products tailored for clinical trials. The electronic data capture (EDC) software combines a user-friendly interface with advanced data capture and management features. The ePRO and eCOA solutions are focused on capturing patient-reported outcomes and clinical outcomes electronically, improving data quality and integrity. Medrio's eConsent product facilitates the management of informed consent, promoting compliance and enhancing the experience for study participants. Their Randomization and Trial Supply Management (RTSM) system helps in managing study supplies and minimizing potential biases. These products aim to provide comprehensive support throughout the clinical trial process.
Medrio Clinical Data Services
Medrio provides comprehensive Clinical Data Services that support diverse data management needs in clinical trials. These services are crucial for managing and analyzing clinical trial data, ensuring accuracy, and adhering to compliance standards. By offering customized data management solutions, Medrio partners with clients to enhance the efficiency of their clinical trials. Their focus on data quality and compliance helps clients navigate the complexities of clinical trial data management seamlessly.
Medrio Regulatory Compliance
Medrio is committed to maintaining compliance with a wide array of regulatory standards, ensuring the integrity and security of their clinical trial solutions. They adhere to international and national regulations including ICH, GCP, FDA 21 CFR Part 11, Annex 11, GDPR, HIPAA & HITECH, CDASH & CDISC, ISO 9001, ISO 27001, and SOC 2. This broad compliance framework underscores Medrio's dedication to providing trusted and reliable solutions in the clinical trial sector.
Medrio Headquarters
Medrio is headquartered at 345 California Street, Suite 600, San Francisco, CA 94104. From this location, the company manages its wide range of clinical trial solutions and services, supporting numerous clients in the healthcare and pharmaceutical industries. Their central location in San Francisco allows Medrio to effectively collaborate with various stakeholders and maintain a strong presence in the clinical trial services market.