Improving readability of clinical trial documents

Have you ever been on the receiving end of your work? I have. Last year, after arriving to the delivery room for the birth of my daughter, I was approached by a doctor with a request to take part in a clinical trial. Although it was very late at night and I was preoccupied with the business at hand, I took her up on her offer. For one, it provided a distraction from contractions. But beyond that, after handling innumerable clinical trial documentation projects over the years, I welcomed the opportunity to find out first hand what it was really like to be a

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6 Responses to “Improving readability of clinical trial documents”

  1. crow says:

    First and formost I would want to know what Big Pharma company was sponsoring the clinical trial. Big Pharma only wants profits and do not care if a person is injured or killed from the trial.

    There is most like a big Pharma company behind the study. I want to know why they are conducting the study, want to know if they WILL DO NO HARM (which I doubt), They are testing the swine flu vaccination on millions of people today. Since there was one done before.

    No way, no how would I volunteer for a clinical study.

  2. admin says:

    Crow,

    Thank you for reading. By law an Informed Consent Form must explain any risks associated with taking part in the study. Unfortunately, in many cases certain risks are not known in advance.

  3. pjbrain says:

    Dear Author aqtext.com !
    Certainly.

  4. graf_edmond says:

    I want to quote your post in my blog. It can?
    And you et an account on Twitter?

  5. Leah says:

    @grad_edmond Thank you for reading.

    Feel free to quote me on your blog, provided that you credit my statements and link back to this site.

    There is a Follow Me on Twitter button on the home page (my Twitter handle is @leah_aharoni)

  6. atv guy says:

    Excellent post thank you!

    Sent via Blackberry

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