Imaging Protocol Development

Comprehensive Protocols Customized to Your Clinical Trial

MMI develops radiographic protocols and image review charters tailored to fit the specific needs of your study. Our comprehensive protocols identify the relevant imaging modalities, acquisition methods, and assessments needed to reliably detect and document the effect of your treatment. Our protocols are based on the latest peer-reviewed research and the expertise of our trained clinical and scientific staff. The following information is typically included in each protocol:

Imaging objectives and endpoints.
Modalities and acquisition methods.
Site qualification and training criteria.
Subject preparation and imaging procedures.
Image labeling and transfer procedures.
Image post-processing and analysis techniques.
Quality control processes and standards.
Data management, reporting, and archival procedures.
Our protocols are high-quality, professionally-produced documents designed for submission to regulatory agencies, IRBs, medical ethics committees, investigators, and others. Our protocols have a successful history of review and approval by the FDA and other regulatory bodies.
Expert Guidance on Endpoint Selection
We provide strategic guidance on the appropriate primary and secondary endpoints pertinent to the imaging assessment. Based on our prior experience with related treatments and knowledge of the scientific literature, we recommend the most relevant success criteria for each endpoint. These criteria are selected to maximize the probability the endpoint will be met. As needed, we provide literature-based justifications to support the proposed imaging endpoints and success criteria for your study. We also maintain constant interaction with your scientific, clinical, and regulatory staff to ensure our recommendations are in alignment with the study requirements and objectives.
Want to learn more? Browse our services and therapeutic expertise, or contact us.
  • Imaging objectives and endpoints.
  • Modalities and acquisition methods.
  • Site qualification and training criteria.
  • Subject preparation and imaging procedures.
  • Image labeling and transfer procedures.
  • Image post-processing and analysis techniques.
  • Quality control processes and standards.
  • Data management, reporting, and archival procedures.

Our protocols are high-quality, professionally-produced documents designed for submission to regulatory agencies, IRBs, medical ethics committees, investigators, and others. Our protocols have a successful history of review and approval by the FDA and other regulatory bodies.

Expert Guidance on Endpoint Selection

We provide strategic guidance on the appropriate primary and secondary endpoints pertinent to the imaging assessment. Based on prior experience with related treatments and knowledge of the scientific literature, we recommend the most relevant success criteria for each endpoint.  As needed, we provide literature-based justifications to support the proposed imaging endpoints and success criteria. We also maintain constant interaction with your scientific, clinical, and regulatory staff to ensure our recommendations are in alignment with the study requirements and objectives.

Want to learn more? Browse our services and therapeutic expertise, or contact us.