THE DESIGN OF THE PROPOSED
IN GENREAL
Title
Title of proposed project
Introduction
Background to research topic, including discussion of previous work in this area
Identification of problem to be addressed, including statement of the hypothesis/ses
Justification of counterfeiting, e.g. why you think this research should be undertaken)
Research Design and details
References



COUNTERFEIT OF PHARMACEUTICAL PRODUCTS IN SAUDI ARABIA


1. Definition of counterfeit medicine and the legislation of counterfeiting through the WHO &FDA & EUROPE.
2. Why to counterfeit medicines?
3. Some data about counterfeit (estimated market in terms of money, of percentage of the genuine products...where they are found? why?
4. Dangers for the health (information's about death toll and illnesses, description of fake medicines
5. Description of a fake medicine and some examples to be given.
6. How to detect them?
A-
 Monitoring the market by MOH and pharmaceutical groups
 Reports by patients ,doctors and hospitals.
 Through Police and Customs
 The important role of Customs (procedures..)
 Monitoring of the Internet
B- pharmaceutical analysis methods.
7. Who is behind this kind of trafficking?
8. What to do against this phenomenon?
The necessary protection by the pharmaceutical groups
At the national level
At the international level


Note: I need in the Research Proposal covers all those points above with Reference from articles and books &WHO & FDA


Footnoting : I DO NOT KNOW WHICH ONE THE ACCEPT IN UK


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