English_ What have i learned freewrite .docx - Benjamin E Conlon Date Course ENGL II COMP CURRENT ISSUE Teacher Schultz Based of the research i have

English_ What have i learned freewrite .docx - Benjamin E...

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Benjamin E. Conlon Date: 4/10/2018 Course: ENGL II COMP CURRENT ISSUE Teacher: Schultz Based of the research i have found through developing my paragraph and my bibliographic annotations i have learned there are various federal clauses and rights that hold certain standards to scientists who involve normal citizens into clinical trials of drugs,products and or otherwise abstract experimentation on the basis that they have consented and agreed to the trails they are participating in. I have learned their are various fda laws thats require not only consent but background health checks for those who have volunteered to participate in drug trials. On the offside i've learned through the format of contract and loopholes that pharmaceutical and other scientific research company can use samples from clinical trials member without consent nor
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Unformatted text preview: reimbursement for specimen. It is also legal for them to share research,results and med information between other doctors,physicians, and journals without verified notarized consent it not established in the contract agreement made by company and negotiated through the clinical trial participant. I've learned about the different human rights having to do with clinical research and what companies are obligated to notify you about and make you aware of prior to considering or beginning a course of clinical trials especially on the basis of systemic drugs taken over a period of time. The side effects,health hazards/risks, and treatment period all need to be notified to the participant upon beginning treatment legally as well....
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