The current global scenario recognizes regulatory medical writing as a tool to for developing authenticated documents related to products undergoing clinical trial. The purpose of regulatory medical writing is to offer the highest quality scientific documents for fulfilling the requirements of particular audience. Regulatory medical writing has grown complex with the introduction of new requirements for drug approval.
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Medical writing is the process of writing scientific or regulatory document by specialized writers known as the “medical writers”. Medical writers might not be the real scientists who did the authentic research, but work with the physicians / scientists concerned in the creation of data, and thereby assist to present that data in appropriate and clear way. The importance of good medical writing must not be ignored as science depends on clarity and accurate reporting, otherwise meticulous research can appear imperfect if poorly presented.
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