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Topic: In vitro (IVF)
a. Develop and construct a timeline showing dates, discoveries, costs, advances, failures, etc.
Step by step
Solved in 2 steps
- Topic/Subject: Research & Evidence-Based Practice Create an informed consent form for the PICO research question below: How does a cancer patient feel about undergoing surgery rather than chemotherapy for faster treatment of the disease?Topic: In vitro (IVF) b. Explain how this technology is supposed to be used to help patients.Outline the general steps from initial drug discovery to IND filing. Add as much detail as you need and feel free to use flow charts, graphics, visuals, as long as is made by you alone and not directly copied-pasted from another source. If an IND is cleared to proceed by the US-FDA, what is the single most important goal of a first-in-human (FIH) clinical trial?
- INSTRUCTION: Write 1 if it's a PURE research and 2 if it's an APPLIED research. NOTE: (no need for explanation) Treat Systemic Lupus Erythematosus (SLE) An investigation into the symptoms of Coronavirus. A research to discover the components of the human DNA. Should vaccinations be avoided to prevent autism? Is genetically modified food hurting health? Is modern technology creating a & quot; dumbing down & quot; of individuals? How do slime molds reproduce? What is the specific genetic code of the fruit fly? How does tobacco use in various forms affect humans? An investigation into the causative factors of malaria.Topic/Subject: Research and Evidence-Based Practice Create an informed consent using the PICO question below: How does a cancer patient feel about undergoing surgery rather than chemotherapy for faster treatment of the disease?Match the following terms/acronyms to their definition below: clinical event committee (CEC), core laboratory, contract research organization (CRO), data safety and monitoring board (DSMB), endpoints, inclusion criteria, power. Characteristics or indications that subjects must have in order to participate in the clinical trial A. DSMB The probability of detecting a meaningful difference, or effect, if one were to occur B. CRO Prospectively identified and quantifiable parameters that a study is designed to meet C. Inclusion criteria An independent organization that provides management services for clinical trials D. CEC An independent body that periodically reviews the results of clinical trials in the US to ensure that patients are not being inadvertently harmed by the study E. Endpoints An independent body that adjudicates clinical events and reports the results to both the trial investigators and the study sponsor F. Power An independent body that…
- Define the following notions and elaborate on their ethical implications: Stem Cell Tourism. Therapeutic MisconceptionRegulations/research help: True or false: Industry-sponsored clinical trials are legally required to only use clinical outcome measures that have been prospectively validated. Which of the following may be true for a significant risk (class III) medical device? (check all that apply) --Is intended as an implant and presents a potential for serious risk to the health, safety, or welfare of a subject --Is purported or represented to be for a use in supporting or sustaining human life and presents a potential for serious risk to the health, safety, or welfare of a subject --Is for a use of substantial importance in diagnosing, curing, mitigating, or treating disease, or otherwise preventing impairment of human health and presents a potential for serious risk to the health, safety, or welfare of a subject --Presents a potential for serious risk to the health, safety, or welfare of a subjectName three reasons a person might turn to complementary and alternative medicine.
- Give laboratory diagnosis and medical managementList 3 possible costs (disadvantages) from this scenario: "Nanotechnology can provide alternatives to early detection of cancer cells, drug delivery, and injectable vaccines that to this day rely on healthcare professionals to administer." Note: COSTS are the setbacks, drawbacks, or negative effects/impacts resulting from the scenario.Create a sample template of the patient medication profile (Note: Do not use the sample found on the internet. You must design your own template.)
