Competition and Regulation in EU Healthcare Markets

What I should do is write an essay answering this question in 4500 words (I need to get a distinction):
‘Medical devices fulfil comparable functions and create comparable risks to human health as pharmaceuticals. It is incomprehensible that they should not be subject to a comparable system of marketing authorisation.’ Identify what are, in your view, the most significant differences between the system for placing medical devices on the market and that for medicinal products and discuss whether you agree that a common approach should be adopted for both categories of products.

What I am asking you to do is providing me with:
– Help with the structure of my essay, i.e. titles and contents for each paragraph. This should contain ALL the relevant issues and should be something on which I can elaborate to do a detailed essay;
– Sources through which I can elaborate on each point;
All the above mentioned should amount to 6 pages, which is what I am paying for. I am attaching to the present message:
1. Outline of the TWO lectures and TWO seminars that tackled the topic of my essay. There you can find SOME of the relevant bibliography. If you have no access to those reading materials on any platform, I can see if I can find some of them somewhere, so feel free to contact me;
2. Power point presentation on the lectures, that you might find helpful.
Anyway, the content of the essay should NOT be exclusively based on this. Moreover, the question of the essay could lead one to include medical data on risks and so on, but this is a law essay, so that some medical data are ok, but only to the extent needed for my legal arguments.
My paper will be checked to see if there is plagiarism, so that I need it to be NOT PLAGIARISED.