CRANIOFACIAL RESEARCH AND STUDY CENTER has its own independent, Institutional Review Board - IRB - accredited and issued by the U.S. Department of Health and Human Services.
Here we can support, supervise and guide both your applications for research and research projeceither if you are regulated by the FDA or not.
Is your project worth it?
How did you determine that this is a research study? Do you have goals, timeline and deadlines set? Do you know what are your regulators in your area? Here is where we can help you set and follow through the standards and requirements of content for your research to comply with your local and general regulatory institutions.
Other than patients data, there are a number of investigations and supportive content that might be helpful and/or required as part of a research project. Also, there are several resources that might be able to supply you with relevant and useful information, in order to make your research project unique.
That cadaver training has changed many aspects of medical education we all know. But there are much more data to be collected and information available every time one specimen becomes available.
Here at the CRANIOFACIAL RSC we use what's called "NON-TRANSPLANT CADAVERIC HUMAN TISSUE" for several purposes, and we strictly follow the requir
That cadaver training has changed many aspects of medical education we all know. But there are much more data to be collected and information available every time one specimen becomes available.
Here at the CRANIOFACIAL RSC we use what's called "NON-TRANSPLANT CADAVERIC HUMAN TISSUE" for several purposes, and we strictly follow the requirements from the regulatory agencies that make sure tissue is safely available for what we do.
Microscopic study and supportive content is a core component of research work and development in healthcare.
Here at the CRANIOFACIAL RSC, we count with qualified and experienced techs to harvest proper material, staining, cross sectioning and sliding of microscopic samples.
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