When the birth control pill was tested in Puerto Rico, this type of experimentation is: Therapeutic Non-therapeutic Clinical trial I O Animal experimentation A and B are correct
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- Informed consent means that aa. nurse has the right to perform a procedure on a patient even if the patient refuses.b. patient agrees to a procedure after being told of the consequences associated with it.c. patient has the right to look at all his or her medical records and test results.d. phlebotomist tells the patient why the test is ordered and the meaning of the results.A colleague asks his friend, a technologist, for the results of his girlfriend’s pregnancy test. The technologist obliged after telling his friend that he is doing him a big favor, and that he should not tell anyone that he told him. The test was positive. The laboratory manager was told about it through another employee. Identify the stakeholders.A manufacturer evaluates a new pregnancy test. The manufacturer enlists 500 study subjects, 190 pregnant females (of whom 150 had a positive test) and 310 non pregnant females (of whom 296 had a negative test). Positive Test Negative Test Pregnant 150 40 Non-pregnant 14 296 Calculate the sensitivity: no references just homework.
- A colleague asks his friend, a technologist, for the results of his girlfriend’s pregnancy test. The technologist obliged after telling his friend that he is doing him a big favor, and that he should not tell anyone that he told him. The test was positive. The laboratory manager was told about it through another employee. What are the values at risk?Which of the following statements can be falsified? a. All of the fish in Lake Michigan are brown. b. French cheese is the tastiest. c. Homeopathic remedies work only if you believe in them.Please answer this in detail question A colleague asks his friend, a technologist, for the results of his girlfriend’s pregnancy test. The technologist obliged after telling his friend that he is doing him a big favor, and that he should not tell anyone that he told him. The test was positive. The laboratory manager was told about it through another employee. What are the moral responsibilities of the laboratory technologist?
- A stapler is used to staple 100 papers, it jams 5 times during the trial. A different brand of stapler performs the same test; it jams 22 times. What is the independent and dependent variables and the control group and the experimental groupA. Plan out design verification for pregnancy test kits medical device 2 and validation -> including strategies for testing, purchase, manufacturing, acceptance criteria, etc. B. propose a Quality System for your manufacturing facility for pregnancy test kits Oh no!Clinical trials can be designed to demonstrate that a new technology offers measurable, relevant benefits, in terms of safety, clinical effectiveness, and in some instances, cost-effectiveness True False
- Given the case scenarion; Write at least 2 or 3 questions that can be ask from the PACU nurse during her endorsement, as a secondary data.A patient is being counseled for possible participation in a clinical trial for a new medication. After the patient meets with the physician, the nurse is asked to obtain the patient’s signature on the consent forms. The nurse knows that this “informed consent” indicates which of the following? a )Once therapy has begun, the patient cannot withdraw from the clinical trial. b) The patient has been informed of all potential hazards and benefits of the therapy. c )The patient has received only the information that will help to make the clinical trial a success. d )No matter what happens, the patient will not be able to sue the researchers for damages.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…