RadMD
RadMD is a provider of imaging solutions for clinical trials, offering customized imaging strategies, total imaging management, independent image analysis, and specialized training through the BRITI institute. They focus on streamlining imaging processes, regulatory expertise, and enhancing trial efficiency to support drug development and clinical research.
Industries
Nr. of Employees
small (1-50)
RadMD
Conshohocken, Pennsylvania, United States, North America
Services
Consulting on design and implementation of imaging strategies tailored to clinical trial goals and agent mechanism of action.
Design of trial-specific imaging endpoints and criteria, including adaptation of existing criteria and development of novel imaging outcome measures.
Operational management of all trial imaging activities including site reads, central reads, image transfers, reporting and final imaging study report creation.
Provision and coordination of expert blinded reviewers for centralized reads and delivery of advanced, quantitative image analyses.
Web-based qualification and training for site readers and investigators, including standardized curricula and site-level technical training.
Support for preparation of imaging components of regulatory dossiers, including medical writing, integrated summaries and coordination with global regulatory authorities.
Consulting on design and implementation of imaging strategies tailored to clinical trial goals and agent mechanism of action.
Design of trial-specific imaging endpoints and criteria, including adaptation of existing criteria and development of novel imaging outcome measures.
Operational management of all trial imaging activities including site reads, central reads, image transfers, reporting and final imaging study report creation.
Provision and coordination of expert blinded reviewers for centralized reads and delivery of advanced, quantitative image analyses.
Web-based qualification and training for site readers and investigators, including standardized curricula and site-level technical training.
Support for preparation of imaging components of regulatory dossiers, including medical writing, integrated summaries and coordination with global regulatory authorities.
Expertise Areas
- Imaging strategy and endpoint development
- Independent central image review and adjudication
- Imaging operations and workflow management for clinical trials
- Regulatory support and submission preparation for imaging
Key Technologies
- Blinded reader training platforms (web-based)
- Centralized reading and adjudication workflows
- Quantitative image analysis methods
- Imaging endpoint specification and protocol integration