During the 2nd Generics Summit sponsored by the DOH last September 7-8, 2011, compulsory licensing (CL) and other intellectual property rights (IPR)-related topics like exhaustion of rights (parallel importation), Bolar Principle, etc. were discussed. See my earlier notes about the summit, Part 12: Expanding Generics, and Part 13: Improving Generics Quality, posted on September 9 and 13, 2011, respectively.
Thailand has seven drugs put under CL covering drugs against hypertension, HIV and some types of cancer.
He mentioned also that RA 9502 has provisions for "Exhaustion of rights" (Art 6 of TRIPS) which is directly linked to "parallel importation". Note that this term is different from ordinary importation. Then there is also the "Research exemption" provision in the law, which allows researchers to use a patented invention like a new drug for experimental or educational purpose.
The "Bolar Provision" or "early working" would allow (mostly local) generic manufacturers to develop a patented drug without the consent of the patent holder. Once the molecule patent expires, the generic producers can instantly market and sell their own branded generics.
Ms. Timmerman's presentation was entitled "Priority Medicines, Essential Medicines for Non-Communioable Diseases". That should be a prelude to the big UN and WHO summit in NYC to control NCDs last September 19-21. One may wonder, why would the UN and many national governments impose more "government responsibility" in healthcare when the decision to over-drink, over-smoke, over-eat, over-sit or not, is mainly personal decision and responsibility.
Also the role of competition among generic producers, but I don't remember that she mentioned competition among innovator companies. And the role of differentiated pricing, which is related to market segmentation and product differentiation.
This list of course is not complete, There should be instances of CL declaration in other countries like India, Pakistan, Ghana, etc.
With the modernization of food (and beverage, tobacco) production and marketing, modernization in people's lifestyle -- they tend to eat more fatty food, gulp more fatty drinks, socialize with friends with more cigarettes, beer and wine -- the development of non-communicable diseases also rise among the people. But this is on top of rising or longer lifespan. Before, people were dying of hunger and lack of food. Now, many people are dying because of too many food and drinks.
If developers of modern drugs that address NCDs are to be demonized as "hungry multinational capitalists who suck sweat and blood from the patients", then who will develop those new drugs and still escape being demonized as such?
The WHO (and many governments) has that ideological baggage of being a silent or implicit anti-innovation, anti-competitive capitalism bias. This could be the main reason why the WHO is always in the forefront of exaggerating certain diseases (before, they exaggerated the threat of HIV, then SARS, H1N1, now the NCDs) as they get more budget and funding from national governments.