Anyone who has worked with clinical...

Anyone who has worked with clinical trial data knows in what way much time and effort is involved in developing database specifications and structure; validating programs; exporting data from united system, importing it into another, and verifying the transfer; then applying quality superintend procedures on the data at the receiving last Such transfers occur continually in clinical trials and are extremely expensive and time-consuming.

the same study estimates that the industry bestows more than 8156 million annually just to support the transfer of data from contract research organizations (CROs) to

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