Integrated Medical Development
IMD is dedicated to supporting the development of medical products through comprehensive clinical research, protocol development, and data management. They aim to facilitate rapid clinical development and commercial success by integrating knowledge, state-of-the-art technology, and regulatory expertise. Their services include clinical trial planning, execution, data management, statistical analysis, and post-marketing safety support, with a focus on efficiency, innovation, and collaboration.
Industries
Nr. of Employees
small (1-50)
Integrated Medical Development
Princeton Junction, New Jersey, United States, North America
Products
Proprietary 21 CFR Part 11-compliant EDC platform
A browser-accessible electronic data capture platform supporting adaptable eCRFs, secure file uploads (device exports, images, PDFs), remote source document review, eDiary integration, and integrations for device data transfer and IWRS.
Proprietary 21 CFR Part 11-compliant EDC platform
A browser-accessible electronic data capture platform supporting adaptable eCRFs, secure file uploads (device exports, images, PDFs), remote source document review, eDiary integration, and integrations for device data transfer and IWRS.
Services
Protocol development
Development of complete clinical trial protocols incorporating clinical, regulatory and site input.
Full-service clinical research organization (CRO)
Planning, execution and reporting of small and medium-sized clinical trials across phases, including investigator recruitment and site qualification.
Data management (21 CFR Part 11 compliant)
Regulated data management using proprietary EDC or paper CRFs, emphasis on CRF design and concurrent data processes to minimize queries.
Electronic data capture platform hosting and customization
Browser-accessible EDC environment with adaptable eCRFs, file upload, and ability to add study-specific modules and integrations.
Interactive Web Response System (IWRS) for allocation and supply control
Web-based treatment allocation, simulation-driven optimization of allocation schemes, and investigational product supply management at sites.
Pharmacovigilance and post-marketing safety services
Call center operations, safety assessments, event documentation, and regulatory expedited reporting processes linked to clinical databases.
Protocol development
Development of complete clinical trial protocols incorporating clinical, regulatory and site input.
Full-service clinical research organization (CRO)
Planning, execution and reporting of small and medium-sized clinical trials across phases, including investigator recruitment and site qualification.
Data management (21 CFR Part 11 compliant)
Regulated data management using proprietary EDC or paper CRFs, emphasis on CRF design and concurrent data processes to minimize queries.
Electronic data capture platform hosting and customization
Browser-accessible EDC environment with adaptable eCRFs, file upload, and ability to add study-specific modules and integrations.
Interactive Web Response System (IWRS) for allocation and supply control
Web-based treatment allocation, simulation-driven optimization of allocation schemes, and investigational product supply management at sites.
Pharmacovigilance and post-marketing safety services
Call center operations, safety assessments, event documentation, and regulatory expedited reporting processes linked to clinical databases.
Expertise Areas
- Clinical trial management
- Protocol development and study design
- Adaptive trial design and statistical simulation
- Clinical data management (21 CFR Part 11 compliant)
Key Technologies
- Electronic data capture (EDC) systems
- Electronic case report forms (eCRF)
- Interactive Web Response System (IWRS)
- Electronic diaries (eDiary)