Answer:
Explanation:
Although it can be helpful to figuring out time of death, or situational matters, there are many variables that go into play. Mainly using it as time of death isn't as precise as decomposition levels or other methods, this imprecision can negatively impacts the case. There are factors that play in digestion and in person to person case that may limit how accurate the stomach content investigation is.
Answer:
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Answer:
ECG paper is a grid where time is measured along the horizontal axis.
Each small square is 1 mm in length and represents 0.04 seconds.
Each larger square is 5 mm in length and represents 0.2 seconds.
Voltage is measured along the vertical axis.
10 mm is equal to 1mV in voltage.
The diagram below illustrates the configuration of ECG graph paper and where to measure the components of the ECG wave form
Heart rate can be easily calculated from the ECG strip:
When the rhythm is regular, the heart rate is 300 divided by the number of large squares between the QRS complexes.
For example, if there are 4 large squares between regular QRS complexes, the heart rate is 75 (300/4=75).
The second method can be used with an irregular rhythm to estimate the rate. Count the number of R waves in a 6 second strip and multiply by 10.
For example, if there are 7 R waves in a 6 second strip, the heart rate is 70 (7x10=70).
An ongoing clinical protocol at your site includes weekly blood draws to assess an exploratory endpoint. Unfortunately, participants are not happy about visiting the clinic weekly, and they are considering dropping out. Therefore, a protocol amendment is being prepared to remove the weekly blood draw. This change can be implemented once the protocol is finalised and submitted to the FDA.
<h3>
What is the FDA?</h3>
The Federal Food and Drugs Act, which was passed in 1906, led to the creation of the Food and Drug Administration (FDA). The organisation is divided into divisions, each of which is in charge of the majority of the organisation's responsibilities relating to food, medicines, cosmetics, animal food, nutritional supplements, medical devices, biological products, and blood products.
The FDA is renowned for its efforts to control the creation of new medications. All new pharmaceuticals must undergo clinical trials, according to regulations set down by the FDA. Before medicines may be offered to humans, pharmaceutical companies must put them through four stages of clinical testing.
To know more about FDA, visit:
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Explanation:
A. HX of any type of cancer
