HCR555 Pharmaceutical Safety and Risk Management
During this course we have covered the technical and regulatory safety aspects of pharmaceutical products. We explored premarket testing and development, recognition of safety signals, post-approval, drug production, risk administration, and administration of pharmaceuticals. Throughout the class you have had opportunities to apply the material covered through participation in discussion boards, assignments, projects and exams. This reflection exercise is an opportunity to explore what you have learned and applied and what it means to you in a professional capacity. Write a reflective essay discussing at least one of the challenges that has been identified during this course regarding drug safety and regulation, and how you could expand upon and use the material from this course to address that challenge in your future career.
Some topics you might want to include are:
Safety analysis and risk-benefit ratio.
Risk mitigation
Conflicts associated with the marketing of pharmaceuticals
Issues related to globalization of pharmaceutical testing and marketing
RUBRIC | |||
Excellent Quality
95-100%
|
Introduction
45-41 points The context and relevance of the issue, as well as a clear description of the study aim, are presented. The history of searches is discussed. |
Literature Support
91-84 points The context and relevance of the issue, as well as a clear description of the study aim, are presented. The history of searches is discussed. |
Methodology
58-53 points With titles for each slide as well as bulleted sections to group relevant information as required, the content is well-organized. Excellent use of typeface, color, images, effects, and so on to improve readability and presenting content. The minimum length criterion of 10 slides/pages is reached. |
Average Score
50-85% |
40-38 points
More depth/information is required for the context and importance, otherwise the study detail will be unclear. There is no search history information supplied. |
83-76 points
There is a review of important theoretical literature, however there is limited integration of research into problem-related ideas. The review is just partly focused and arranged. There is research that both supports and opposes. A summary of the material given is provided. The conclusion may or may not include a biblical integration. |
52-49 points
The content is somewhat ordered, but there is no discernible organization. The use of typeface, color, graphics, effects, and so on may sometimes distract from the presenting substance. It is possible that the length criteria will not be reached. |
Poor Quality
0-45% |
37-1 points
The context and/or importance are lacking. There is no search history information supplied. |
75-1 points
There has been an examination of relevant theoretical literature, but still no research concerning problem-related concepts has been synthesized. The review is just somewhat focused and organized. The provided overview of content does not include any supporting or opposing research. The conclusion has no scriptural references. |
48-1 points
There is no logical or apparent organizational structure. There is no discernible logical sequence. The use of typeface, color, graphics, effects, and so on often detracts from the presenting substance. It is possible that the length criteria will not be reached. |
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HCR555 Pharmaceutical Safety and Risk Management