The recent H1N1 pandemic reinforces the need to heed the recommendations in the guidelines, which outline the complementary roles and responsibilities of WHO and national authorities at the onset of an influenza pandemic. For example, WHO strongly recommends that all countries establish multidisciplinary National Pandemic Planning Committees to develop strategies appropriate for their countries

in LGK-974 price advance of the next pandemic. Because of the higher morbidity and mortality associated with seasonal influenza in the very young and the elderly, Mexico included vaccination against influenza as a priority in 2004 and offered free vaccination for all children under 3 years and adults over 60 years of age. Since then, the use of influenza vaccine in our country has increased gradually to reach nearly 23 million doses in 2010

(Fig. 1). In 2007, the Mexican General Board of Health decreed the establishment of a multisectoral Operational Alectinib mouse Strategy within the National Preparedness and Response to Pandemic Influenza Plan, and instructed Birmex, a state-owned company, to take immediate action to develop domestic production of seasonal and – if needed – pandemic vaccine against influenza. At that time, Birmex considered three different alternatives. The first was to develop in-house technology to develop and market influenza vaccine. However, the lengthy time frame to license a vaccine, including preclinical and clinical trials, raised concerns that a pandemic could occur before a vaccine became available. Since the primary objective of the Government was to protect the population, the success of this option could not be guaranteed. A second alternative was to acquire the technology. Even though this may have combined the benefits of owning the technology and reducing the delay to the launch of a vaccine, we were unable

to identify a willing technology provider. The third, adopted alternative was to establish a joint venture with an internationally recognized vaccine company that would be committed to establish the whole production process in Mexico. Under a technology transfer agreement signed in 2008, sanofi pasteur became our technology partner. For its part, sanofi pasteur agreed to build a facility in Ocoyoacac to produce the antigen DNA ligase and, pending completion of the facility, assure the supply of 30 million doses of seasonal vaccine per year. In addition, should an influenza pandemic occur before vaccine production in Mexico became operational, sanofi pasteur would make pandemic vaccine available to the Government of Mexico. The responsibility of Birmex was to build a Good Manufacturing Practice (GMP)-compliant facility to formulate, fill and package (FFP) the seasonal – and eventually pandemic – influenza vaccine. To this end, a site in Cuautitlan was acquired.