Clinical Genomics Consulting (CGC) provides state of the art support for laboratory developed testing.  Our services are focused on accelerating growth of diagnostic and translational sciences companies.  By providing access to proven capabilities for regulatory support, validation of testing and market analytics, CGC provides solutions to bring your IVD to market.

 

We can help your lab develop CLIA and CAP protocols, work with you towards CLIA Licence submission and initial surveys, provide site audits, and work with you to create standard operating procedures, and other necessary tools to make your business function at its maximum efficiency. In addition, we can help design the necessary validation to begin offering LDT's through your laboratory. Our professionals are able to assist you with the development of science-to-lay-person business documents. We are also able to connect you with biostatisticians to provide you with assitance in reviewing your data.

 

To inquire about our full range of services and pricing, please contact us.