Clinical Research Philosophy
cyberDERM Clinical Studies has over 40 years of experience as a contract research organization specializing in developing and validating new methods, as evidenced by the deep publication histories of our investigators and Dr Gary Grove's status throughout the industry as a key opinion leader. We excel at executing standard protocols, your company's custom protocol, or developing our own protocol from the ground up to meet your company's needs. In tandem with cyberDERM Technical Center we are able to choose and/or develop the best instrumentation or photographic systems to fit your needs. Dr Charles Zerweck and Mr Tim Houser are both experienced expert graders with over 50 years of combined grading experience. Our staff also excels at developing and executing appropriate self assessments to accurately measure subjective parameters which are important to your product development and marketing strategy. We consider this 3-pronged approach to be the highest standard, ensuring that our study results are meaningful and robust.
Protocol Development. Whether we are working from a standard protocol, one provided by a sponsor, or developing our own, our focus is on preparing a clear and concise road map to ensure successful study execution. We take a comprehensive approach, including the leaders of every team within cyberDERM in the process. From subject recruitment to statistical analysis, you can be sure that your study has been designed in a thoughtful manner to best fit your needs.
Execution. Our qualified and experienced staff excel at preparing for and executing your study to the highest standard, in compliance with applicable FDA regulations, ICH guidelines, the protocol, and our own Standard Operating Procedures. Our staff are well trained, with documentation, to perform their assigned tasks while much of our technical and scientific staff provide instrumental training to technicians from across the industry. Our technical equipment is maintained to the highest standard, with documentation of regular maintenance and calibration as needed, as well as daily performance and calibration checks. cyberDERM Technical Center is also available on site to repair or replace instrumentation as needed making it highly unlikely for us to ever be in a situation where we cannot perform the assessments as outlined in the protocol for technical reasons.
Analysis and Reporting. At the completion of a study our team is prepared to quickly analyze all data, perform statistical analyses, interpret results and provide a draft report in a timely fashion. Throughout the entire study, from protocol development to final report generation, Quality Assurance and Quality Control are proactively ensuring proper documentation, data handling study execution and reporting. At the end of each study our principal investigators can confidently stand behind any conclusions made as being meaningfully supported by the data.
Protocol Development. Whether we are working from a standard protocol, one provided by a sponsor, or developing our own, our focus is on preparing a clear and concise road map to ensure successful study execution. We take a comprehensive approach, including the leaders of every team within cyberDERM in the process. From subject recruitment to statistical analysis, you can be sure that your study has been designed in a thoughtful manner to best fit your needs.
Execution. Our qualified and experienced staff excel at preparing for and executing your study to the highest standard, in compliance with applicable FDA regulations, ICH guidelines, the protocol, and our own Standard Operating Procedures. Our staff are well trained, with documentation, to perform their assigned tasks while much of our technical and scientific staff provide instrumental training to technicians from across the industry. Our technical equipment is maintained to the highest standard, with documentation of regular maintenance and calibration as needed, as well as daily performance and calibration checks. cyberDERM Technical Center is also available on site to repair or replace instrumentation as needed making it highly unlikely for us to ever be in a situation where we cannot perform the assessments as outlined in the protocol for technical reasons.
Analysis and Reporting. At the completion of a study our team is prepared to quickly analyze all data, perform statistical analyses, interpret results and provide a draft report in a timely fashion. Throughout the entire study, from protocol development to final report generation, Quality Assurance and Quality Control are proactively ensuring proper documentation, data handling study execution and reporting. At the end of each study our principal investigators can confidently stand behind any conclusions made as being meaningfully supported by the data.
Clinical Research Services
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Breathability
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Bio-mechanics
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Eye Puffiness
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Anti-Aging
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