Added by Geoff Sauer on Mar 02, 2003.
Average rating: 3.00/5.00 (n=2, std dev: 1.41)
 


The pharmaceutical industry must develop, test, and market all drugs according to strict regulations. To get a drug licensed, records of what procedures were done and whether they were compliant with the relevant requirements must be written. These are sent to the regulatory authorities who determine whether the drug should be approved for use in humans. Examples of regulatory documents written by medical writers.
 
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