Let me ask you, the CMA, and others a question. I'm still searching for answers around the proper process to ensure the access to information and transparency of information that you've all espoused, especially from the drug companies, which are a problem by all accounts. I'm sure you're not going to disagree with that. Some of the recommendations include an open-access website that would have all drug approvals and non-approvals on it, as well as a summary of and the rationale behind the decision; a complete review of all clinical trial data used to reach a decision made available to the academic community; and finally, an independent board to provide oversight of the regulatory process and keep it accountable.
Are there any objections to any of those three suggestions?