FEBRUARY 2016
www.bdo.com
AN ALERT FROM THE BDO TECHNOLOGY & LIFE SCIENCES PRACTICE
LIFE SCIENCES
CYBER ALERT: FDA ISSUES NEW
CYBERSECURITY GUIDELINES FOR
MEDICAL DEVICE MANUFACTURERS
Following a spate of major data
breaches — resulting in over 112
million compromised health records
in 2015 alone — healthcare is the
latest industry to face heightened
regulatory scrutiny of its cyber
preparedness.
The Cybersecurity Act of 2015, a provision
of the omnibus spending bill passed in
December, requires the Department of
Health and Human Services (HHS) to
submit a report to Congress assessing the
preparedness of the healthcare industry
in responding to cyber threats within the
next year, with the goal of establishing a
“single, voluntary, national, health-specific
cybersecurity framework.” As part of this
mandate, HHS must create a cybersecurity
task force comprised of regulatory agencies,
industry stakeholders and cyber experts to
help (1) plan a single system for the federal
government to share intelligence regarding
cybersecurity threats to the healthcare
industry, and (2) recommend protections for
networked medical devices and electronic
health records.
On the heels of the bill’s enactment, the
U.S. Food and Drug Administration (FDA)
has issued a new set of draft postmarket
guidance for the management of
cybersecurity in medical devices, outlining
recommended steps medical device
manufacturers should take to address
growing cybersecurity threats and minimize
risk to patients.
SUMMARY
In a follow-up to its October 2014 premarket
cybersecurity guidance, the FDA’s draft
guidance addresses recommendations
for managing postmarket cybersecurity
vulnerabilities for marketed devices,
advocating for a risk-based and proactive
approach. While the guidance is primarily
aimed at manufacturers, it notes that
medical device cybersecurity is a shared
responsibility between all healthcare
stakeholders including healthcare facilities,
patients and providers.
The FDA encourages manufacturers to
embrace “good cyber hygiene” through
ongoing risk assessment and monitoring,
routine device cyber maintenance and
implementation of necessary actions to
mitigate device functionality and patient
safety risks. In addition, the agency promotes
information and intelligence sharing (a key
provision of the Cybersecurity Act of 2015)
within the medical device community.
“Voluntary” participation in an Information
Sharing Analysis Organization (ISAO)
is considered a critical component of a
manufacturer’s proactive cyber strategy and
is considered a mitigating circumstance when
an issue arises.
The FDA calls for manufacturers to adopt
a comprehensive cybersecurity risk
management program and documented
process for identifying hazardous cyber
vulnerabilities in line with the National
Institute of Standards and Technology
HOW DO I GET MORE
INFORMATION?
For more information about how
medical device manufacturers and
healthcare organizations can improve
their cybersecurity preparedness,
please contact:
SHAHRYAR SHAGHAGHI
BDO Technology Advisory Services
National Practice Leader
sshaghaghi@bdo.com
RYAN STARKES
BDO Life Sciences Practice Leader
and Assurance Partner
rstarkes@bdo.com
DAVID FRIEND
BDO Chief Transformation Officer and
Managing Director of BDO’s Center
for Healthcare Excellence &
Innovation
dfriend@bdo.com
PATRICK PILCH
BDO Healthcare Advisory Practice
Leader and Managing Director
ppilch@bdo.com
MAURICE LIDDELL
BDO IT Security & Infrastructure
Services National Leader
mliddell@bdo.com
DALE TIMMONS
BDO Management and Technology
Advisory National Leader
dtimmons@bdo.com
Read more ïµ
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BDO KNOWS LIFE SCIENCES
Framework for Improving Critical
Infrastructure Cybersecurity, which includes
the core principles of “Identify, Protect,
Detect, Respond and Recover.” Such a
program should include:
u Monitoring cybersecurity information
sources for identification and detection of
cybersecurity vulnerabilities and risk;
u
Understanding, assessing and detecting
presence and impact of a vulnerability;
u
Establishing and communicating processes
for vulnerability intake and handling;
u
Clearly defining essential clinical
performance to develop mitigations that
protect, respond and recover from the
cybersecurity risk;
u Adopting a coordinated vulnerability
disclosure policy and practice; and
u
Deploying mitigations that address
cybersecurity risk early and prior
to exploitation.
When evaluating potential cyber risks,
manufacturers should focus on assessing
the risk to the device’s “essential clinical
performance” and consider the following:
1) exploitability of the cybersecurity
The
vulnerability.
2) he severity of the health impact
T
to patients should the vulnerability
be exploited.
In instances where the “essential clinical
performance” of a device could be
compromised, the manufacturer is required
to notify the agency. Reporting requirements
are not enforced if the following
circumstances are met:
1) known serious adverse effects or
No
deaths associated with the vulnerability.
2) he manufacturer sufficiently remediates
T
the issue within 30 days of learning of the
vulnerability.
3) he manufacturer is a participant of
T
an ISAO.
A device with an unacceptable level of risk
to its essential clinical performance may
be considered in violation of the Federal
Food, Drug & Cosmetics Act and subject to
enforcement actions.
BDO INSIGHTS
The FDA refers to medical device
cybersecurity as a “shared responsibility.” We
often talk of “multi-factor authentication”
and “layered defense” as core cybersecurity
strategies, and the same lens should be
applied to the entire healthcare ecosystem.
While manufacturers are ultimately
responsible for identifying and remediating
potential cyber vulnerabilities associated
with their medical devices, hospitals
and healthcare systems must safeguard
their networks from potential breaches
of security via medical devices. Medical
device manufacturers are only the first line
of defense.
The domino effect of a healthcare data
breach sheds light on the importance of
information sharing, a growing area of
focus in cyber strategy and policy. The
Cybersecurity Information Sharing Act
(CISA), also part of the omnibus spending
bill, offers prescriptive advice on furthering
collaboration between the government
and private sector, as well as industry
collaboration within the private sector.
While we will likely see an uptick in threat
intelligence sharing across all industries,
concerns about protecting competitive
information and privacy risk have yet to be
addressed.
The level of sharing remains to
be seen, and will dictate the effectiveness of
ISAOs and other information sharing systems
in mitigating cyber risk. Participation in
ISAOs or Information Sharing and Analysis
Centers (ISACs) will likely remain voluntary
in the near-term; however, as exemplified by
the FDA, regulatory entities will increasingly
consider participation when assessing
cyber preparedness.
Healthcare organizations and medical device
manufacturers are well-advised to seek
assistance from consultants and technology
specialists experienced in developing risk
management frameworks and strategies to
navigate complex security and compliance
issues. BDO has deep experience in the
medical device and healthcare industries and
assists companies in conducting security risk
assessments, testing controls, conducting
security monitoring and developing and
executing on incident response plans, in
addition to implementing cybersecurity
risk management programs, strategy
and governance.
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