there is a revolution underway in the way we treat cancer.
instead of the traditional “cut and burn” approach to cancer treatment, precision medicine — or precision oncology — is allowing us to take targeted aim at tumours, reducing side effects and damage to healthy cells, as well as increasing the odds that the treatment works. it also means that the right cancer treatment gets to the right patient, at the right dose, at the right time. there’s more potential than ever before for cancer patients to live longer, enjoy a better quality of life and, most importantly, survive this devastating disease.
except that for many canadians who live with cancer, complex regulatory and approval pricing models and fragmented health-care systems make these innovative therapies impossible to access. this needs to change.
complex approval processes cost lives
one of the biggest barriers is the long and complicated regulatory approval process for new therapies in canada — especially compared to other oecd countries. an overly bureaucratic process wraps clinical trial design and monitoring in red tape, slowing health canada approvals. the result is canadians who are denied treatments that are already available in other parts of the world, like the united states or europe.