Export this Abstract | Print this Abstract | Add to my preferred Abstracts list | My preferred Abstracts list (1) | Back to Search
Analysing the reports on counterfeit and sub-standard medicines
- In: G9 - Information sharing to address counterfeit and substandard medicines on Monday, 5 September 2005, 14:00-17:00
- At: Cairo (Egypt) (2005)
- Type: Presentation
- By: NICHOLSON, Jane (Industrial Pharmacy Section, Regulatory Affairs, Slough, United Kingdom)
- Abstract:
When companies acquire a sample of a product that could potentially be counterfeit from either pharmacists, consumers or other party, analysts at the manufacturers’ laboratories should run tests to examine the components of the medicine and determine whether it is a fake. If it is, this should be reported to the National Government Authorities
.. The access to the whole abstract and if available the presentation file is available to FIP members and to congress participants of that specific congress.
Please login
Last update 28 September 2023