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CRO Laboratory Services

Specimen Testing

Technology Transfer

Technology Transfer of a qualified or validated assay can take place at either the client's laboratories or at Cambridge Biomedical, where the assay can be run under CAP/CLIA or GLP quality levels. Samples may also be aggregated, stored under required conditions and run later in a batch mode to minimize costs.

Cambridge Biomedical has client-tested Technology Transfer procedures that allow assays developed or optimized at our laboratory to be transferred efficiently to you. Our staff is actively involved in every stage of the process, from your scientists observing the assay at our facility to our scientists actually running the first sample batches onsite in your laboratory.

We can also work with our clients to provide proficiency and accuracy testing on an ongoing basis. Our CLIA certified, CAP accredited, and FDA registered laboratory is capable of running under GLP guidelines, and allows assays to be transferred from the development group and to be routinely run in support of your clinical trials.