Mr. Speaker, all the documents referred to in that report were before Mr. Justice Krever. He looked into all of the facts and, in fact, they were referred to in his report.
The report this morning on the radio was factually wrong in important respects. I encourage the member to look at the facts.
It was alleged that there was no action taken until 1993. In fact, Health Canada issued a directive in 1991. It said this morning that Health Canada awaited a U.S. study. That is false. Health Canada instructed manufacturers to start screening plasma a full two years before the publication of the U.S. report. The Health Canada directive was issued five months before the FDA acted.
The facts were—