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Canfield is the industry leader in providing the imaging systems and support necessary for quality photographic documentation. Whether used as supporting documentation or directly for clinical efficacy, quality images and related data can make the difference in today's competitive and time sensitive clinical trial process.
Medical photographic monitoring
Canfield provides comprehensive centralized monitoring services and currently supports all phases of the clinical development process. Our project management team ensures sites maintain compliance with all aspects of a clinical trial's imaging protocol. We provide support on an ongoing basis to study sites worldwide. We can create study specific instructions in any language and provide training at Investigator meetings or at clinical sites.
Images received by Canfield are logged, monitored, checked for quality, and archived using validated and 21 CFR Part 11 compliant software and systems. This provides a complete audit trail of clinical documents from receipt at Canfield through the archiving process. For the ultimate in turnaround, study images received may be viewed near real time by sponsors or sites through the use of Canfield's clinical web services.
To help site staff better understand the technical issues within their images, Canfield provides feedback through the use of photographic result reports. In addition, Canfield can provide proactive visit tracking and can also act as a "gatekeeper" to ensure proper inclusion criteria are met at screening.
Canfield's experienced staff provides full equipment technical support and inventory control of study supplies.
Training
Most people can take a snapshot, but properly trained site staff can provide the best medical photographic result… reproducible serial photography. Don't let improper training compromise the quality and usefulness of your photographic documentation. Canfield can provide training and training materials for use in Investigator meetings, on-site staff training, and webinars.
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