A well-understood tenet exists among the FDA and other regulatory bodies: if you didn't write it down, it didn't happen! And if it didn't happen, your company stands to lose time, money, and perhaps its competitive edge. This book provides writers with the tools they need to put effective documentation in place. It offers a broad range of documents representative of the types of writing in the healthcare industry, from the laboratory and QA to manufacturing and regulatory affairs. The book offers valuable insights into managing systems and producing documentation that meets the requirements of the binding regulations.
Sprache
Verlagsort
Verlagsgruppe
Zielgruppe
Für Beruf und Forschung
Für höhere Schule und Studium
Maße
Höhe: 229 mm
Breite: 152 mm
Gewicht
ISBN-13
978-1-57491-088-9 (9781574910889)
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Schweitzer Klassifikation
Autor*in
Industry Consultant, Flanders, New Jersey, USA
Chapters include
Writing Within the Regulatory Environment
Connecting Writer and Reader
Organizing and Delivering Information
Writing Letters and Memos
Preparing Routine Reports
Process Reports
Periodic and Progress Reports
Developing a Clear Style. Building Strong Sentences. Verb Tenses in English
Punctuating Effectively
Word Usage