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ASPIRE Independent Review Board Announces 10 Ways to Protect Participants' Rights in Clinical Drug Trials and Optimize Results From Research
Date:6/9/2008

life," states Mercie Madrid. Another participant, Mike Means, says, "I participated in a clinical trial for Psoriasis and my condition improved dramatically."

ASPIRE IRB's 10 Ways to Protect Participants' Rights and Maximize Results for Clinical Research
1) Participants can decide not to participate in the research study with

NO penalty or loss of benefits any time.

2) Participants can ask any questions that occur before, during or after

the study.

3) Be Informed. Get a copy of the consent form, the main source of

information for the study.

4) Ask the principal investigator as many questions as needed to

understand the trial.

5) No legal rights are waived by signing a consent form.

6) Ethical and legal codes governing medical practices apply to clinical

trials.

7) Be prompt to all scheduled appointments.

8) Call the research facility if there is a reaction to a drug or device

immediately.

9) Follow the study related instructions that are given to you.

10) Certain studies may expect more visits than regular care. This may

affect employment.

About ASPIRE IRB http://www.aspire-irb.com

ASPIRE IRB is a privately owned certified Women's Business Enterprise headquartered in San Diego, CA. They oversee clinical research studies. They review and approve any research involving human participants with the aim to protect their rights and welfare. Their goal is to make sure the protocol is well-designed and the risks are as minimal as possible. ASPIRE has overseen clinical drug trials for Cancer, Psoriasis, Schizophrenia, Depression, Multiple Sclerosis, Pain, Obesity, Dermatology, Heart Disease, Diabetes, Hyperactivity, Alzheimer's Disease, Sleep Disorders, Garlic, supplements and more. Clients include: Pfizer, Covance, PPD, Takeda, Sanofi-Aventis, Wyeth, Charles River, MRA and
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SOURCE ASPIRE IRB
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