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How do governmental agencies manage regulatory risks within the Health System?

Topic: How do governmental agencies manage regulatory risks within the Health System?
15000-20000 words excluding appendix
FEEDBACK ON DRAFT:
Draft feedback:
Thanks for starting writing this. However, the introduction that was sent to me does not follow what was intended with this project.
HSE was not the subject of the study, had done my research interviews to two regulators, the Medicines and Healthcare Products Regulatory Agency (MHRA) which regulates the use of medicines in the UK and the Human Tissue Authority (HTA) which regulates human tissue.
I am also required to compare at least two regulators. What is your objective in this dissertation???
Can you get back to me as soon as possible, as we need to think about what it’s gonna be done going forward. As it stands at the moment it needs more references and a good definition of what the dissertation is going to achieve. The reason I sent you my proposal was because it explained exactly what needed to be done in this dissertation.

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Calcium and phosphorous

Topic: Calcium and phosphorous

Sources MUST be peer reviewed OR from original papers, NO WEBSITES AND NO BOOK.
.
Attached Files:
1-Sample from a student (contains several pages (scanned (jpg) (not word document), numbered with number and letter ex 1 b, 2 b … etc).
P stands for page No. for example p 2b means page number 2b.
2- A file called randox calcium.
3- A file called randox phosphorous.
Steps: PLEASE KEEP THE SAMPLE INFRONT OF YOU AND FOLLOW THESE STEPS:
1- Introduction (see sample page 2 b and do the same introduction (I mean same info but DIFFERENT SOURCES. And please be within the context of the sample introduction. Also you may need to extend some info ( Maximum 3-4 lines) If you required.
2- Aim (p 2b) do it the same but with Paraphrasing.
3- Materials and method, standard concentrations, QC values, reference intervals and both ca/cr ratio and p/cr ratio (p 2b and p 3b) JUST COPY TEXT (NOT TO BE Paraphrased).
4- Calcium procedure and Assay principle (p 3b) Just Paraphrase it From the sample and/or The original assay instruction pdf file (called randox calcium).
5- phosphorous procedure and Assay principle (p 3b and p 4b) Just Paraphrase it From the sample and/or The original assay instruction pdf file (called randox phosphorous).
6- Creatinine procedure and Assay principle (p 4b) Just Paraphrase it From the sample ONLY.
7- Results (p 4b) Just Paraphrase it CAREFULLY From the sample.
8- TABLE 1, TABLE 2 AND TABLE 3 (p 4b and p 5b) JUST DRAW BLANK TABLE (INCLUDE TEXT ONLY, NOT TO WRITE NUMBERS)
9- Under table 3 (p 5b) there are text, JUST PARAPHRASE IT CAREFULLY.
10- DISCUSSION (THE MOST IMPORTANT PART (EQUAL 60%) (p 5b AND P 6b) (NEED IT MORE STRONGER THAN THE SAMPLE ONE) here just see the sample and do it in the SAME way (careful paraphrasing + paying attention to change THE in text references and replace it with NEW reference/s that SAID the SAME information. i.e. LINKING FINDINGS TO INFO
11- References List (p 6b) Simply put your references (Please I need at least 6) Vancouver Style . i.e. You may use one or 2 from sample reference list.

 

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Medical terminology

Medical terminology (read all files to know more about the topic an what you should do)
I need medical glossary but the way of doing for this order is different so I will upload 2 files which have the instruction and how to do the work. please read them carefully and if you have any question please email it to at any time
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Proton pump inhibitors

Topic: Proton pump inhibitors

Proton pump inhibitors
The assignments must be
• Create a news report
• Create a captivating heading . You may use images to create a captivating title of your Pharmacology news.
• Provide an in-depth discussion on various aspects
1 – clinical uses of the drug or drug class,
2– associated risks and benefits
3– specific areas of concern
4– clinical studies where applicable
5 – events or attributes leading to controversy or new therapy.
6– Changes to registration, availability, or recommendations that may have subsequently occurred, if applicable.
• Reflect on the importance of ongoing clinical trials and post-marketing surveillance with registered drugs.
-Written assignment Double sided
– TWO A4 PAGES plus references
– References to include Initial Reference Search (25 minimum credible resources ) References Cited in Report
-Vancouver style referencing
– Word count 1000 (excluding references) you must Include word count in the report
The topic must be have an excellent
1-Presentation
2– Spelling and grammar
3 – Introduction (background)
4– Body (scientific merits)
5– Conclusion
6- Literature research and use of references
7– Vancouver style referencing WITHOUT PLAGIARISM
I will upload some assignments for example to know the structure which I need

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Fatty acid in red blood cells as a potential biomarker for diagnosis of Amyotrophic Lateral Sclerosis(ALS)

Fatty acid in red blood cells as a potential biomarker for diagnosis of Amyotrophic Lateral Sclerosis(ALS)”
Aim and objective of this study is to analyse RBC fatty acid profile and find changes in ALS patients compared to healthy volunteer.
I want the write up and analysis of my result section and even discussion section (Both Result and Discussion) for my dissertation. For analysis of my result spss software is used and will be attaching the spss data plus the output please have a look in my result output if i have done it correctly or wrong plus my supervisor have asked to “Correct multiple comparison” for testing the significance. According to the result write down the discussion supporting the result and whether the objective of this study is fulfilled or not.