REPORT OF THE COMMITTEE |
FRIDAY,
December 14, 2001 |
The Standing Senate Committee on Social Affairs, Science and Technology
has the honour to table its
FOURTEENTH
REPORT
Your
Committee, which was authorized on Thursday, March 1, 2001 to examine and report
upon the developments since Royal Assent was given during the Second Session of
the Thirty-Sixth Parliament to Bill C-6, an Act to support and promote
electronic commerce by protecting personal information that is collected, used
or disclosed in certain circumstances, by providing for the use of electronic
means to communicate or record information or transactions and by amending the
Canada Evidence Act, the Statutory Instruments Act and the Statute Revision Act,
now tables its report.
Background
In
November 1999, the Committee held extensive hearings in consideration of Bill
C-6, today known as the Personal Information Protection and Electronic
Documents Act 2000, S.C. c. 5 (hereinafter the Act). At these
hearings, witnesses representing the health sector demonstrated a lack of
unanimous support for the Act as presented. Their primary concern was the
possible impact of the Act on their ability to collect, use and disclose
personal health information and hence on their ability to keep the health system
functioning efficiently and effectively.
The
Act imposes obligations on organizations with respect to the collection, use and
disclosure of personal information within the course of commercial activities.
The responsibility for oversight, redress and audit under the Act rests with the
Privacy Commissioner.
The
substantive obligations created by the Act are contained in the Canadian
Standards Association Model Code. The Code is incorporated by
reference in section 5(1) of the Act, thus giving it the force of law. The Model
Code was said to have been developed through five years of negotiation among
stakeholders primarily in the business community; however, the evidence before
the Committee in 1999 suggested that the health sector had not participated
sufficiently in the negotiation of the Model Code and, therefore, it did
not reflect the realities of that sector.
For
that reason, and in recognition of the importance and complexity of the issues,
the Committee recommended that Bill C-6 be amended to suspend the collection,
use and disclosure of personal health information from the application of Part
1. The government accepted the recommendation and amended the bill with the
addition of section 30.(1.1). That section, which created a one-year suspension,
was proclaimed in force January 1, 2001, (SI/2000-29). As such, the Act will
begin to apply to personal health information on January 1, 2002.
Observations
and Recommendations
The
Committee is aware that, since 1999, discussions have been ongoing between
certain health sector stakeholders and government to clarify and resolve these
issues. These discussions did not
reach a definitive conclusion, although significant progress has been made.
The
Canadian Institutes of Health Research (CIHR) considered the issues over a two
year process of background work and consultations among relevant stakeholders. This process has resulted in recommendations in the form of
draft regulations, which it has submitted to the Committee for its consideration
(Appendix 1). The Committee has
considered the regulations proposed by CIHR, and commends CIHR for its efforts
in this regard. The Committee supports the intent of the proposed regulations. The Committee is confident that these
regulations will receive their fullest and fairest consideration in those
discussions in the relevant forum.
As
well, the Privacy Working Group, a discussion forum consisting of some
stakeholders in the health sector, has informed the Committee that it was able
to make some progress towards achieving consensus within the sector by focussing
its discussion on the principles underlying the privacy of health information
(Appendix 2). While the discussion did not produce a unified position, it did
result in agreement on many issues, including a process to address the
unresolved issues. The Working Group expressed the view that that process would
require the active involvement and leadership of the federal government.
However, in a letter to the Canadian Medical Association (Appendix 3),
the government made it clear that the concerns of the Privacy Working Group
should be resolved between the members of the group and the Privacy
Commissioner.
In
a letter of November 20, 2001 to the Chairman of the Committee (Appendix 3), the
Privacy Commissioner undertakes to maintain “vigilant oversight” in order to
ensure that personal health information is collected, used and distributed only
as appropriate. To this end, he states his intention to interpret sections
7(2)(c) and 7(3)(f) of the Act in a broad manner, with a view to ensuring that bona
fide health research is not deterred or impeded. We have carefully
considered the timely and judicious intervention of the Privacy Commissioner and
we are satisfied that the approach he proposes will provide assurance that
individuals’ privacy rights will be protected, while at the same time ensuring
that organizations will be able to collect, use and disclose personal
information for health research purposes in appropriate ways. However, the
Committee is of the view that regulations such as those proposed by CIHR may nonetheless be necessary to
provide greater clarity and certainty of the law and to ensure that its
objectives will be met without preventing important research to continue to
better the health of Canadians and improve their health services.
Also, further guidance and direction is needed in respect of the
provision, management, evaluation and quality assurance of health services.
The
Committee is also mindful that, pursuant to section 29(1) of the Act, Part I
will be subject to review by a committee of Parliament five years after its
coming into force.
In light of all these considerations, the Committee is of the view that its further intervention is not warranted at the present time. Nevertheless, it is the Committee’s intention to actively monitor the discussions, as well as the approaches and solutions, which emerge. Perhaps more importantly, the Committee recognizes that the privacy issue needs to be addressed in the context of the development of the electronic health record (EHR). The Committee is on record as strongly supporting the rapid development of the EHR. At the same time, the Committee is very mindful of the potential risks to the privacy of personal health information, which arise as a result of the creation of an EHR. The Committee hopes to work with all interested parties in seeking a solution that appropriately balances the need for privacy with the need for an EHR.
Respectfully submitted,
MARJORY
LEBRETON
Deputy Chair