Description
- Question 2: Poor Data Collection Methods
- Paragraphs: 2 (5-7 sentences each)
- References: Yes
- Criteria:
- In your opinion, describe two (2) major consequences of inaccurate and/or poor collection of data in clinical trials
- Describing indicates you will need to 1) introduce the topic, 2) identify each major consequence, 3) analyze the consequence in terms of type of risk (and for who), 4) provide one or more examples and 5) ground your critical thoughts in evidence.
- Question 3: Limited eCRF Responseso Paragraphs: 2 (5-7 sentences each) o References: Yes o Criteria: § One of the drawbacks of electronic case report forms is the limitation on the number of responses a coordinator can enter § An example might be an eCRF that asks for a subject’s gender and then limits the response to male or female § Problem: how does the coordinator “code” transgender? o Provide another example of a data variable that might limit responses on an eCRF
o Describe the variable: § how is it used § what responses are standard (ex: male versus female) § why do you think limited responses might be a problem – apply synthesis, analysis and evaluation of the evidence o Note: remember to start your post by introducing the topic. Don’t assume readers will “just know” what you are talking about.
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