stay up to date on this topic
the pride canadians feel toward the country’s health-care system has declined in recent decades. beyond the well-documented doctor shortages and overcrowded hospitals, patients are experiencing lengthy delays in getting access to the innovative medicines they need.
canadians wait two years or longer before getting access to health canada-approved new treatments and vaccines through public drug plans. that’s almost double the wait times of other developed countries around the world.
as a result, canada ranks last in the g7 nations and 19th out of 20 organization for economic co-operation and development (oecd) member countries in the time it takes for approved new medicines to become accessible to patients.
“for rare disease patients, the numbers are even more staggering,” says alison sargent, chief of staff and vice president of operations at innovative medicines canada. “only 60 per cent of rare disease treatments make it into canada, and most get approved up to six years later than in the us or europe.”
for sargent and many of her industry peers, the importance of improving canada’s health care takes on a more personal meaning. sargent’s 11-year-old daughter suffers from phenylketonuria, a rare disease which can lead to serious brain injuries when not properly managed by a strict diet. as the mother of a child suffering from a rare disease, sargent fully understands the importance of being able to access cutting-edge new treatments, quickly.
a long and inefficient process
these delays in accessing new drugs are due to the complex and sequential nature of canada’s drug access system, with inefficiencies at nearly every step of the process. after a drug receives health canada approval, health technology assessments are conducted to make funding recommendations for public drug plans.