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
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.
Interactive Web Response System (IWRS)
Treatment allocation and test agent supply control system providing simulation for optimization of treatment allocation schemes.
eCRFWeb V3
Electronic case report form software platform for clinical trials.
Electronic Case Report Form (eCRF)
An adaptable data collection purpose eCRF that can be updated with minimal downtime and used in combination with uploaded source documents for remote site monitoring.
G6Vue
DexCom Authorized Data Transfer application providing Continuous Glucose Monitoring (CGM) data collection and alert functionality.
Electronic Diary
An extension of the eCRF deployed with real-time data capture to enhance the quality and quantity of acquired data.
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.
Interactive Web Response System (IWRS)
Treatment allocation and test agent supply control system providing simulation for optimization of treatment allocation schemes.
eCRFWeb V3
Electronic case report form software platform for clinical trials.
Electronic Case Report Form (eCRF)
An adaptable data collection purpose eCRF that can be updated with minimal downtime and used in combination with uploaded source documents for remote site monitoring.
G6Vue
DexCom Authorized Data Transfer application providing Continuous Glucose Monitoring (CGM) data collection and alert functionality.
Electronic Diary
An extension of the eCRF deployed with real-time data capture to enhance the quality and quantity of acquired data.
Services
Development of complete clinical trial protocols incorporating clinical, regulatory and site input.
Planning, execution and reporting of small and medium-sized clinical trials across phases, including investigator recruitment and site qualification.
Regulated data management using proprietary EDC or paper CRFs, emphasis on CRF design and concurrent data processes to minimize queries.
Browser-accessible EDC environment with adaptable eCRFs, file upload, and ability to add study-specific modules and integrations.
Web-based treatment allocation, simulation-driven optimization of allocation schemes, and investigational product supply management at sites.
Call center operations, safety assessments, event documentation, and regulatory expedited reporting processes linked to clinical databases.
Development of complete clinical trial protocols incorporating clinical, regulatory and site input.
Planning, execution and reporting of small and medium-sized clinical trials across phases, including investigator recruitment and site qualification.
Regulated data management using proprietary EDC or paper CRFs, emphasis on CRF design and concurrent data processes to minimize queries.
Browser-accessible EDC environment with adaptable eCRFs, file upload, and ability to add study-specific modules and integrations.
Web-based treatment allocation, simulation-driven optimization of allocation schemes, and investigational product supply management at sites.
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)
News & Updates
Critical information path
IMD identifies key information necessary to advance clinical development at critical junctures, including iterative human factors testing for devices and biomarker establishment for drugs.
Electronic Data Capture (EDC) for All Data Collection through 21 CFR Part 11
IMD offers proprietary applications accessible via internet browser with a single login, supporting secure document distribution, file transfer, and adaptable eCRF functionalities.
Trial Design and Adaptive Features for Efficiency
IMD designs efficient trials with adaptive methodologies, including adaptive allocation, sample size, and sequential designs, with support for regulatory negotiations.
Post Marketing Product Safety / Pharmacovigilance
IMD provides safety support services including call centers, safety assessments, regulatory reporting, and software tools for seamless collaboration.
Special Purpose EDC Functionalities
Includes product safety applications, CGM data collection, medication dose adjustment algorithms, and proprietary insulin dosing algorithms.
A prospective observational study evaluating V-Go® in type 2 diabetes patients.
Critical information path
IMD identifies key information necessary to advance clinical development at critical junctures, including iterative human factors testing for devices and biomarker establishment for drugs.
Electronic Data Capture (EDC) for All Data Collection through 21 CFR Part 11
IMD offers proprietary applications accessible via internet browser with a single login, supporting secure document distribution, file transfer, and adaptable eCRF functionalities.
Trial Design and Adaptive Features for Efficiency
IMD designs efficient trials with adaptive methodologies, including adaptive allocation, sample size, and sequential designs, with support for regulatory negotiations.
Post Marketing Product Safety / Pharmacovigilance
IMD provides safety support services including call centers, safety assessments, regulatory reporting, and software tools for seamless collaboration.
Special Purpose EDC Functionalities
Includes product safety applications, CGM data collection, medication dose adjustment algorithms, and proprietary insulin dosing algorithms.
A prospective observational study evaluating V-Go® in type 2 diabetes patients.