NUR 699 GC Week 4 Discussion2: protection of human subjects 

Conducting research projects while ensuring the protection of human subjects is necessary. What are some methods to protect personal rights of someone in one of the groups that is labeled as vulnerable? Justify your rationale.

You must proofread your paper. But do not strictly rely on your computer’s spell-checker and grammar-checker; failure to do so indicates a lack of effort on your part and you can expect your grade to suffer accordingly. Papers with numerous misspelled words and grammatical mistakes will be penalized. Read over your paper – in silence and then aloud – before handing it in and make corrections as necessary. Often it is advantageous to have a friend proofread your paper for obvious errors. Handwritten corrections are preferable to uncorrected mistakes.

Use a standard 10 to 12 point (10 to 12 characters per inch) typeface. Smaller or compressed type and papers with small margins or single-spacing are hard to read. It is better to let your essay run over the recommended number of pages than to try to compress it into fewer pages.

Likewise, large type, large margins, large indentations, triple-spacing, increased leading (space between lines), increased kerning (space between letters), and any other such attempts at “padding” to increase the length of a paper are unacceptable, wasteful of trees, and will not fool your professor.

The paper must be neatly formatted, double-spaced with a one-inch margin on the top, bottom, and sides of each page. When submitting hard copy, be sure to use white paper and print out using dark ink. If it is hard to read your essay, it will also be hard to follow your argument.

MORE INFO 

protection of human subjects

Introduction

The FDA is responsible for ensuring that medical devices and their associated clinical studies meet the safety and efficacy standards required under federal law. The agency enforces regulations that protect human subjects from harm, including through its oversight of clinical trials.

Priorities

Protecting human subjects is a top priority.

Protecting the public is also important, because we want to ensure that all people have access to quality healthcare in a safe environment. This means protecting both patients and staff from harm, as well as protecting property from damage or theft. It’s also important that we treat animals humanely so they can live out their lives in comfort and happiness—this ensures that no animal has to suffer for research purposes alone!

In order to protect both humans and animals, some testing may be necessary. However, it is important that the research team has a thorough understanding of what they are testing for, how they plan to implement those tests, and how they plan to ensure that their research methods are ethical and legal.

Consequences for human subjects protections violations

• Disqualification from federal funding for research.

• Loss of clinical privileges.

• Loss of institutional affiliation.

• Loss of employment, including your position and benefits.

• Loss of license to practice medicine in the United States (including Puerto Rico).

This includes being unable to do research or receive training that requires you to have a license; this also includes having your medical license revoked by any state board or regulatory agency regulating medical practice in that state/territory where you currently reside or worked previously; this also means not being able to practice medicine anywhere else either domestically or internationally without special approval from either NIST’s Office on Human Development Research and Training & Education Program Development Division or NIST’s Administration Office—both located within our Main Campus Building 3rd Floor Conference Room B1002 at 700 South Federal Street NW Washington DC 20897-3025 USA phone number 202-357-4246 email address hdrof@nistcenetworkincorporation

Conducting clinical trials with devices

Conducting clinical trials with devices is important for a couple of reasons. First, it’s a way to help improve the safety of medical devices, which in turn can help prevent injuries and save lives. Second, conducting clinical trials with devices may be a necessary step in bringing those devices to market—if you’re going to put your product on the market at all!

Of course, there are also some ethical implications associated with conducting clinical trials with medical equipment: What if you don’t have enough time or money to conduct adequate testing? What if your device breaks easily because someone didn’t test its durability properly? That’s why it’s important that these questions be asked before getting started (and also why they shouldn’t be ignored).

Learn about the rules and regulations in place to protect human subjects.

Learn about the rules and regulations in place to protect human subjects. Learn about the consequences for human subjects protections violations. Learn about conducting clinical trials with devices.

The term “clinical trial” refers to a research study that tests the safety and/or effectiveness of a new drug or device in humans. Clinical trials help determine whether a treatment is safe for people, and how well it works.

Conclusion

You should be aware that there are many regulations in place to protect human subjects. If you’re working on a project that involves clinical trials or devices, it’s important to know what rules and regulations apply so that you can follow them properly.