At
а national level, each country should develop appropriate medicines policy
options, legislation, and enforcement strategies in view of its own situation
and availability of institutional framework, professional and financial
resources. The policies should aim at involving the Government, its agencies,
the pharmaceutical industry, drug importers and distributors, the
pharmaceutical profession, governmental organizations, public interest groups
and consumer groups, etc in efforts to prevent the supply of counterfeit
medicines. Measures are often effective when carried out by all concerned
working together.
More
specifically, governments of each country should show political will/commitment
for evolving and implementing programs for combating counterfeit medicines.
Political will and commitment should be demonstrated by:
- enacting new drug laws or updating existing drug laws for prohibiting counterfeit medicines;
- establishing institutions for the regulation of medicines and clearly setting out in the drug laws, the power, duties and responsibilities of the institution(s);
- training of personnel, including enforcement officers, for national drug control;
- making available necessary financial and other resources;
- ensuring that the drug laws are enforced; and
- fostering international cooperation in the control of pharmaceuticals and entering into bilateral and multilateral agreements with other governments and with international organizations such as WHO, Interpol and the World Customs Organization (WCO).
Judicial
procedures and policies should reflect the seriousness of the problem and the
offence. Courts should speedily dispose of cases involving counterfeit
medicines and impose appropriately severe penalties on convicted offenders. 1n
addition, courts should order the confiscation/forfeiture and destruction of
counterfeit medicines.
Combating
counterfeiting of medicines is а shared responsibility to which all interested
parties have to contribute. Non-governmental organizations or community based
organizations such as consumer associations should be informed about the
problem of counterfeiting and the possible presence of counterfeit drugs in the
national distribution chain. They should be provided with information and
methods for detection so that they are able to report cases to the national
drug regulatory agencies.
The
general public should be encouraged to become involved in the fight against
drug counterfeiting. Education and information campaigns directed at the
general public should be established and the public should be advised to buy
medicines from legitimate sources rather than from peddlers and hawkers or from
market places and streets. Consumers should also be encouraged and advised to
report to their prescribers or physicians any lack of improvement in their
health status in spite of the treatment or any adverse reactions experienced.
More
privatization and liberalization of the world economy, more extensive opening
of borders to trade and increased promotion and sale of drugs through the
internet are going to lead to increased circulation of counterfeit drugs in
national and international markets. This means greater cooperation between countries
at subregional, regional and international levels will be needed to combat
counterfeit drugs in the future. Cooperation should include developing common
strategies, timely exchange of information and harmonization of measures to
prevent the spread of counterfeit drugs. Cooperation would improve if all
countries adopt а common definition of counterfeit drugs.
At
а global level, а more effective response to the threat of counterfeit drugs
could be the development of an international convention to control trade in
counterfeit and substandard drugs
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