Thank you, Mr. Chair.
As mentioned, I'm here with my colleague, Dr. Guillaume Poliquin, and also Christian Roy from the Department of Justice.
Members, I want to begin with the steps we've taken to respond to your motion of March 31.
We've reviewed the relevant documents and worked very hard in a short period of time to prepare the package of documents that will assist you in your study. As I indicated in my letter to your law clerk, Monsieur Dufresne, we've redacted documents where the information pertained to personal information, investigations or security matters. The reason we've done so is that as public servants we're bound by law to keep confidential information confidential. It's not that we're wishing to be unco-operative or unresponsive; we are disclosing as much as we can within the limits of the law.
The Government of Canada's guiding document, entitled “Open and Accountable Government”, has been used for many years to explain the obligations of witnesses before a parliamentary committee. I note in particular the passage in Annex E:
Public servants also have a duty to hold in confidence some of the information that comes into their possession in the course of their duties. There is a tension between that obligation and the request of parliamentarians for disclosure of that same information. When appearing before parliamentary committees, public servants should refrain from disclosing that kind of confidential information, for instance because the information is confidential for reasons of national security or privacy.
That's Annex E of “Open and Accountable Government”.
Consistent with this guidance, in good faith, we've considered how to find ways to respond to the requests for information from the members of the committee within the limitations that we're bound to uphold. These include my obligation under the Privacy Act, which is legislation enacted by Parliament in the House of Commons to protect against the disclosure of personal information and the infringement of the privacy and rights of individuals.
In compliance with that advice, we have applied redactions to protect certain sensitive information. Accordingly, I'll do my best to assist the committee in this study while refraining from divulging information that ought to remain confidential on various grounds. I have no authority to disclose any additional information to you. As you'll see, the limitations on what we can disclose are consistently well documented throughout the package of materials that we've provided to you, which include public communications and documents previously disclosed under the access to information process. The limitations that guided those documents remain in place.
Here's what we can say about the two matters we discussed last time.
You've received many records from the Public Health Agency related to the transfer of Ebola and Henipaviruses from the National Microbiology Laboratory to the Wuhan Institute of Virology in March 2019. The basic chronology of the transfer can be found at page 111 of the package provided to your law clerk. These records demonstrate that when sharing these samples, the NML followed normal internal guidelines and all applicable requirements under the Human Pathogens and Toxins Act, or HPTA, and regulations, as well as the Transportation of Dangerous Goods Act, TDGA, and regulations related to it and the Canadian Biosafety Standard.
Here's how a transfer normally works. The NML routinely receives and shares samples with other public health laboratories to contribute to the advancement of science. Transfers follow strict protocols, including the requirements I just mentioned, as well as NML standard operating procedures. The NML has detailed procedures outlining the steps required for transferring risk group 4 pathogens in accordance with the transportation of dangerous goods regulations. These include detailed procedures outlining step-by-step roles and responsibilities for all involved in the shipment, what documentation is required by the NML and from the receiving laboratory, when to initiate an emergency response assistance plan—an ERAP—notification, as well as how to package the samples. Approvals are required at various steps throughout the process, from the initial transfer authorization to the specific shipping details.
The shipping process for risk group 4 pathogens is outlined under the mandatory ERAP. The plan assists local emergency responders and describes what to do in the unlikely event of a release of materials while they're in transit.
Regarding the March 2019 transfer, documentation of the necessary approvals is evidenced in pages 265 to 271 of the English package, including the NML transfer authorization. A number of the emails relate to the ERAP that was put in place for the shipment, such as at page 132.
However, full redactions were done to the laboratory certification and the letter from the director of the laboratory, as this was third party information.
You will note reference to material transfer agreements, MTAs. It's important to understand that an MTA was not in fact required for virus transfers at the time. An MTA is not a safety requirement but a document that provides a mechanism for transferring controlled materials from one party to another, primarily to safeguard intellectual property rights. As such, IP experts are consulted to determine whether an MTA is required.
While this is the only time we have shared virus samples with this particular lab, collaborations with labs outside Canada are critical to advance public health research into infectious diseases. PHAC's National Microbiology Laboratory is internationally renowned for its scientific excellence and its contributions to global health.
This maximum containment laboratory has a long-standing international reputation for sharing materials for the purpose of advancing scientific knowledge. Given our standing as a WHO collaborating partner for viral fever viruses, as well as our knowledge of regulations and standards for these types of transfers, the laboratory in Winnipeg is often asked to provide materials to new or existing programs, including laboratories in the United States. The NML is open to providing materials to other labs in a safe, responsible and transparent fashion to foster global collaboration rather than enable research on any given disease to be monopolized by specific teams. This is a component of advancing public health research and science aimed at improving public health on a global scale.
You will notice that one of the individuals named in the motion was involved in this transfer. Regarding the situation of the two individuals named in the motion, we have already confirmed that they no longer work for the NML. We have also mentioned that there had been an administrative investigation. We cannot discuss the nature of the administrative investigation, its scope, or its findings. That said, to avoid undue inferences, I want to state again, as is evidenced throughout the documentation that you received, that the fact that the transfer of the viruses took place—which, again, was done in compliance with internal policies and proper approvals—is not connected to the departure of the two employees.
As you know, there is also an RCMP investigation. I cannot comment on that matter, and questions should be directed to the RCMP.
I am happy to take your questions about these documents and answer them as best I can.
Thank you very much.