| Accuracy in our content and presentation is a CLD corporate value. All materials undergo internal reviews, fact checking, and quality control procedures before they are sent to our clients. Strict referencing of medical information to primary sources and extensive experience with client medical/legal/regulatory committees allows our materials to navigate our clients' approval systems with a minimum of revision. In addition, our extensive writing experience streamlines the process by allowing us to know what to include, what to leave out, and how to write with fair balance for the FDA and other approval bodies.
Our online materials go through extensive QA and QC, and we test all electronic materials on the laptop computers and other assorted peripherals used by our clients. All this is done with strict attention to deadlines and client requirements for LMSs and LSMSs. We begin early in the process so that, by the end, our materials can be rapidly deployed to meet client needs.
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