Order Number |
m876tfde32 |
Type of Project |
ESSAY |
Writer Level |
PHD VERIFIED |
Format |
APA |
Academic Sources |
10 |
Page Count |
3-12 PAGES |
Hey everyone,
I believe that for a Crisis Management Plan to be efficient it needs to give instructions that are clear, concise, and detailed. Basically it needs to be simple enough that even a small child will be able to understand it. Additionally, all risks need to be scanned in order to identify any potential threats and/or vulnerabilities. Furthermore, the plan needs to be constantly revisited and updated to any changes. It would make no sense to have the same plan for one year if the environment changes every few months. That would only be setting up the plan for failure. Everyone needs to know their role in the plan and the only way to really do that is through training and exercises. After everyone is efficient in the plan they would only need to exercise the plan once a month (Britton, 2020).
I believe my group is amazing. At first it was difficult, because nobody wanted to pick their tasks; however, now that the tasks are assigned, I believe that everyone is motivated and working very efficiently to the best of their abilities. At this time I don’t have any questions or concerns for the class, but I would like to express my gratitude and say it was an honor to go through this class with you all, and I hope we have future courses together.
After taking this class I believe that the best way to respond to a lone active shooter is to send as many police to him or her as possible while making as much noise as possible. I’m Military Law Enforcement, and that’s what we’re taught, but a reason stands behind it. Statistics have proven that most active shooters kill themselves when they hear the presence of responding officers. I don’t want to sound insensitive or mean, but I would rather the active shooter kill themselves than to harm innocent people.[Order Now]
Very Respectfully,
Joseph Turner
Pharmaceutical Sciences Discussion
QUESTION 1
drug name : ADALIMUMAB
Long Research Project: pharmacodynamics sources: Find pharmacodynamics information for your target medication to add to your draft report. For this assignment you will merely need to submit a list of properly cited sources that provide key information on the pharmacodynamic properties of your drug of interest, including the interactions critical to the drug’s mechanism(s) of action. This will help you prepare for the submission of your next paper draft in Week 10.
See the Assignment5_Rubric.pdf for grading criteria.
This assignment must be typed and submitted electronically in MS Word (.doc or .docx) or PDF format. The file must be named in the following format: Lastname_Assignment5.doc. Submit your completed document to Assignment 5, listed on the Modules and Assignments pages, as a file attachment.[Order Now]
QUESTION 2
DRUG: AMLODIPINE
Long Research Project: pharmacodynamics sources: Find pharmacodynamics information for your target medication to add to your draft report. For this assignment you will merely need to submit a list of properly cited sources that provide key information on the pharmacodynamic properties of your drug of interest, including the interactions critical to the drug’s mechanism(s) of action. This will help you prepare for the submission of your next paper draft in Week 10
QUESTION 3
Create your initial post in response to the following:
Discuss regulatory controls in place for supplements and homeopathic medications.
Reply:
Regulatory controls have had substantial growth for both supplements and homeopathic forms of medications. The Food, Drug, and Cosmetic Act of 1938 carried out procedures to help the growth as well as set regulations for both the supplements and homeopathic. When discussing homeopathy within the United States the forms of medications have to also go through clinical trials. Homeopathic products have the same requirements for approval as other drugs. Rather than how normal supplements and medications work homeopathic forms of medications do not need to be approved through the FDA. The FDA has not reviewed this form of medication for safety and effectiveness. There just needs to have full manufacturing information to create production under the Federal Food, Drug, and Cosmetic Act.