regulatory affairs department uses all 25 packs (60%) are most commonly used. Due to the need for paper documents and to copy multiple dosing information for filing at least.
Regulatory affairs department all the 25 packs (60%) are the most commonly used because it requires a lot of paper on the preparation of drug literature, and multiple copy. The FDA approved for filing
Regulatory affairs department uses all 25 packs (60 % ), there is a need to use as much paper in the preparation of documents and information must be submitted to the copy for multiple applications.