Thank you again, Mr. Chair.
Just to go back, I was looking this up online. According to ISED's website, we have 2% of the world's pharmaceutical market, but we attract 4% of clinical trials. Clinical trials, though, are a really important way for patients to get access to drugs that are not approved in Canada or are not for public reimbursement.
Has the PMPRB done any work, or any internal analysis, on what the expected drop in clinical trials will be—over the next, say, one to five years—if these regulations go through, or are they expected to increase? Have you done that analysis? Also, what will the impact be on patients and patient access to some rare-disease drugs, like rare oncology drugs, in Canada?