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THE RILEY REPORT – March 2003from Thomas B. Riley (Tom@Rileyis.com) Following is the Riley Report for March 2003. Please feel free to pass this on as you see fit. If you wish to use any or part of the Report in an offline publication please acknowledge the author or contact the author if to be fully republished offline. If you are not currently subscribed to the Riley Report (there is no charge) you can email
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This month's report
is from guest correspondent David Keeshan, a specialist in health privacy.
In his article he examines some recent developments relating to the
application of Canada’s federal Personal Information Protection and
Electronic Documents Act (“PIPEDA”) to health information.
A case currently before the Federal Court of Canada points out that some
very basic foundational questions have yet to be resolved in determining what
constitutes “personal health information” for the purposes of that Act. That case will have significant consequences for the
non-consensual disclosure to third parties of prescription-related data by
pharmacies for commercial purposes. It
also suggests that the Courts will take an expansive view of who can use
PIPEDA’s enforcement mechanisms, with the result that privacy challenges by
business competitors may become common. The
Report draws on material written by David Keeshan which appears in the most
recent issue of Health Privacy in Canada: Law, Practice and Compliance.
David is a lawyer and the co-author of, among other things, The Law of
Search and Seizure in Canada, 5th Edition, The Police Guide to Search
and Seizure, and Privacytown. Health
Privacy in Canada: Law, Practice and Compliance is published 8 times per year by
Electric Law Press (http://www.electriclawpress.com).
Breaking
New Ground: Applying PIPEDA to Health Information
The
federal Personal Information Protection and Electronic Documents Act (“PIPEDA”),
which received Royal Assent on April 13, 2000, governs the collection, use and
disclosure of personal information by private sector organizations in the course
of commercial activity. It
incorporates, as a schedule, the 10 Fair Information Practices set out in the
Canadian Standards Association Model Code, and creates an oversight and
enforcement mechanism involving the Federal Privacy Commissioner and the Federal
Court. The
legislation has a three phase implementation process.
In the first phase, in force January 1, 2001, the Act was applied to the
collection, use and disclosure of personal,
non‑health related information in the course of commercial activity by
organizations under federal constitutional
jurisdiction, or to the personal information of employees in connection
with the operation of a federal work, undertaking or business.
The second phase, in force January 1, 2002, added health related
information. As of that date,
pursuant to s. 30(1.1), personal health information collection in the federal
sphere was required to meet PIPEDA’s requirements. In the third phase, which
will commence January 1, 2004, the Act will apply to all organizations that
collect personal information - including health information - in the course of
commercial activity under both federal and provincial jurisdiction.
Organizations which, at that time, are governed by “substantially
similar” provincial legislation, will be exempted from the application of the
Act in respect of the collection, use or disclosure of personal
information that occurs within that province. One
of the most interesting questions being raised with respect to PIPEDA is:
How will it be applied to personal health information? Of
all kinds of personal information, health related data is perhaps the most
sensitive and raises the greatest privacy concerns for citizens.
A case currently before the Federal Court of Canada, involving IMS Health
Canada, Ronald Maheu and the Privacy Commissioner of Canada, points out that
some very basic foundational questions have yet to be resolved in determining
what constitutes “personal health information” for the purposes of the Act. It also sheds some light on how the Courts may interpret the
Act. Some
background is helpful. Pharma
Communications Group Inc. and IMS are competitors in the business of selling
prescription information written by doctors to producers of prescription drugs.
In September, 2001, the Privacy Commissioner of Canada rejected a complaint by
Ronald Maheu, the principal of Pharma Communications, under PIPEDA that IMS
Health Canada had breached the Act by selling information about the prescribing
practices of physicians, without their consent.
Maheu argued that IMS had purchased a number of items of information from
Canadian pharmacies taken off prescriptions without the knowledge or consent of
the prescribing doctor. This information was said to include store number, drug
identification number, drug name, drug strength, manufacturer, selling price,
new or refill, reasons for use, reasons for no substitution order,
prescriber’s first and last name, phone number, and patient gender and date of
birth. The Commissioner took the view that an individual
prescription, though potentially revealing about a patient, “is the outcome of
the professional interaction between the physician and the patient...and should
be regarded as a work product ‑ that is, the tangible result of the
physician’s work activity.” As
a “work product” that prescribing information was not personal information
and hence PIPEDA did not apply. Maheu
then turned to the Federal Court, alleging that the Privacy Commissioner was
wrong in determining that information collected and disclosed by IMS was not
personal information under the Act. The
litigation raised two significant issues with respect to the interpretation of
PIPEDA. First, it addressed
the fundamental issue of whether doctors’ prescribing data is personal
information and therefore protected by the Act, or, whether it is a
non‑personal work product as characterized by the Privacy Commissioner.
Should the Federal Court overturn the Privacy Commissioner’s findings,
it would have significant implications for the non‑consensual collection
and use of doctor and patient prescription information.
Secondly,
it raised the question of whether PIPEDA can be used by businesses to challenge
the data use practices of competitors. Because
failure to follow fair information practices could reduce costs and deliver a
competitive advantage, it is conceivable that the Courts would permit
applications by other businesses or interested third parties.
As its statutory description makes clear, PIPEDA is, after all, primarily
e‑commerce legislation. That
second issue was at the forefront when IMS subsequently moved to strike out the
application as an abuse of process or, alternatively, to require Maheu to post
security for costs under Federal Court R. 416(1)(g) on the basis that he was "impecunious and the proceeding
frivolous and vexatious."
IMS's motion was heard by a Prothonotary, an officer of the
Federal Court who, while not
a judge, has duties of judicial
nature, including dealing with interlocutory work and even taking trials in
minor matters. In May 2002, the
Prothonotary ruled that (a) a very
stringent standard applied to striking
an action, and while it would appear to be an
abuse, or vexatious or frivolous to use PIPEDA to obtain a competitive
business advantage, the application shouldn't be struck in the absence of
decided cases bearing on the scope of PIPEDA; (b) a less stringent standard
applied to applications for security for costs and the material gave reason Maheu
appealed the Prothonotary’s order, and in an important procedural ruling, the
Federal Court (Trial Division) held that the Prothonotary misinterpreted PIPEDA
when he came to the conclusion there was reason to believe that Maheu’s
application for review was for an improper purpose, i.e. an attempt to obtain a
commercial advantage over IMS. Lemieux
J held that the scheme of PIPEDA is to establish a set of rules applicable to
organizations that collect, use or disclose personal information in the course
of commercial activities. It is a public law regulatory statute providing for
the means of enforcement through complaints, the Privacy Commissioner’s
investigation and report, and an appeal by the complainant as of the right to
the Federal Court, which may make orders in the nature of public law remedies.
Maheu was seeking from the Court, as he had a right to do, a
determination whether IMS’s practices comply with the law in terms of relevant
collection gathering techniques involving personal information, in particular
paragraph 4.3.5 of the Schedule to PIPEDA. It did not matter that Maheu’s
personal information was not at stake in the complaint he made to the Privacy
Commissioner. That consideration was irrelevant. The complainant was not Pharma Communications, but rather an
individual, Maheu, who had a right to apply to the Federal Court, Trial Division
for a hearing following the determination that his complaint was not well
founded. As
well, disqualifying a competitor from access to PIPEDA’s enforcement
mechanisms was not in Parliament’s contemplation having regard to the
fact that it is competitors engaged in commercial activities who, along with
persons whose personal information is being collected, are primarily affected by
its rules. The action was therefore not frivolous and IMS was not entitled to
security for costs from Maheu. Unless
it is overturned, the Trial Division ruling helps clarify how, and by whom,
PIPEDA’s enforcement mechanisms can be used.
It suggests that the Courts will take an expansive view of who can use
PIPEDA’s enforcement mechanisms, with the result that privacy challenges by
business competitors may become common. The
failure to follow fair information practices could reduce short term costs and
potentially deliver a competitive advantage.
By allowing competitors standing to enforce PIPEDA, the courts may
facilitate a much more dynamic use of the statute. The
ruling also permits the case to move forward s so that the federal Court can
deal with the substantive issue, namely whether prescription data is in fact
personal health information, or whether, as the Privacy Commissioner suggests,
it is a work product that the Act is not intended to regulate. For further
information on this issue go to: Electric
Law Press (http://www.electriclawpress.com).
Thomas Riley is available for consultations, preparation of reports, presenting workshops or delivering speeches at conferences and seminars on e-government, e-governance and e-democracy. Please contact me at the email address below for further details.
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