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INTRODUCTION
Medical writing is the activity of presenting often-complex scientific information in a clear and concise manner to a target audience and has gained an increasingly important place in the drug development process as companies look for faster, more efficient ways to bring new drugs to the market. Medical writers employed in the pharmaceutical industry work in two broad areas: regulatory and marketing. The majority of medical writers' work is regulatory and includes investigators' brochures, investigational new drug applications, protocols, subject information and informed consent forms, clinical study reports (CSRs), abstracts, manuscripts for publication in medical or scientific journals, common technical documents, and regulatory summary documents. Medical writers are generally responsible for drafting the scientific content as well as the format and presentation of each document and therefore require broad scientific, regulatory, and medical knowledge and an ability to assimilate key information on new therapeutic areas. This broad skill set, combined with a keen eye for detail and an ability to organize large amounts of information, enables medical writers to be valuable reviewers of the various clinical and statistical documents written by other project team members. Indeed, medical writing is now recognized as a specialist field and as a vital component of high-quality drug submissions (1). |
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Writing
a records and information management (RIM) request for proposal (RFP)
can be a significant undertaking that will require resources from many
different departments, including those responsible for original
documents, records management, support areas such as IT, and key
stakeholders with corporate compliance and budget responsibility.
An RFP effort will typically begin when a department identifies a
need. For example, the IT department may be assigned to research and
implement a records management system (RMS) that will work seamlessly
with existing document creation software, as well as with existing
paper records. The business requirements that are driving the project
may involve compliance with regulations such as the Sarbanes-Oxley Act
(SOX) and the Health Insurance Portability and Accountability Act
(HIPAA), as well as with accounting issues.
Planning should begin with understanding the variables that may
exist for the RIM opportunity. These are only a few of the questions
that should be asked during the planning stage to help the organization
understand what technologies will be required for an RMS and what
solutions may be possible.
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AMS: Let's talk about Edinburgh first of all. We both write about
the same place, but in different ways. John Rebus's Edinburgh is a
relatively bleak, dark place.
Why do you focus on that side to the city?
IR: I think of Edinburgh being a Jekylland-Hyde place -- with an
elegant, beautiful, rational new town and a higgledypiggledy, slightly
chaotic, half-buried old town. It's an absolutely brilliant setting for
a crime novel because it almost seems as if there's a dark side to the
geography, not just to the criminals' characters.
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It’s not easy to write a white paper. And reading them can also be quite a challenge!
Unfortunately, many white papers are difficult to digest and come
across as though slightly ‘nerdy-types’, locked in research labs,
prepared them with very little consideration for their readers.
So, if you’re about to write your first white paper, here are a few golden rules to follow...
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Spelling mistakes and grammatical errors in
your technical content will reflect poorly on your company. In some
cases it may even lose you potential customers. So, good editing and
proofreading is an important aspect of all good technical content
writing. So, before you publish a new or revised article on your
technical site, you should remember to take time to double-check your
work. In today’s world when mistakes are really costly, you need to
proof read the articles for your technical site carefully to ensure
that there are no embarrassing errors in it.
While, technical content proofreading make sure that all the
quotation marks and parentheses are in place. Another thing to check is
the punctuation. Is punctuation spaced consistently? And, for technical
content, you should not double-space the sentences like it’s normally
done in traditional typing. Also, make sure that the page numbers in
the Table of Contents match the locations of the articles? It would be
embarrassing for you, not to mention annoying for the browser if the
page numbers in the table of contents don’t match the location of the
articles.
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Rejection is never easy. But some authors
can't separate themselves from their work, and take rejection letters
very personally. I get many emails from disgruntled writers who can't
get past their anger to figure out why their work was turned down in
the first place. So before you spend hours sticking pins in your editor
voodoo doll, see if you recognize yourself below:
The complaint: "Editors practice age discrimination. I'm over 50 and editors believe only young authors can write for children."
The truth: Editors are interested in finding good books, period. It
doesn't matter how old the author is. Take a look at the lists of award
winners (ask your librarian, or do an Internet search for Caldecott or
Newbery Awards) and note the ages of the authors. Many didn't start
writing until their kids were in school full time, or took up writing
as a second career. Editors also know that the best stories come from
years of life experience, and older writers have more to draw from.
Yes, occasionally a book written by a teenager will make the news, but
more often than not it's the novelty of the author's age that gets the
publicity, not the quality of the writing. And why does the editor know
your age in the first place? There's no reason to mention it in your
cover or query letter, unless it has direct bearing on the story. If
you're writing historical fiction and you actually lived through the
events in the plot, or your nonfiction book is based on years of study
in the subject, then your age is a plus.
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