Dear Colleagues:
Is there any kind of "plain-language" sub-group in RAPS?
My colleagues and I are committed to make our company's regulatory submissions more reader-friendly and accessible, and we know the FDA likes them that way. (They have told us so -- and besides, under the Plain Language Act of 2010,
they are supposed to write in plain language as well.)
So I am seeking a forum or meet-up within the RAPS community, where we can discuss how to improve our own skills in this area, and how to make plain-language communication more prevalent across the regulatory world.
Any thoughts? Thanks,
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Key Payton
Medical Writer
United States
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