Philips delivers Q2 sales of EUR 4.4 billion, with 6% comparable
sales decrease; income from continuing operations of EUR 213
million, Adjusted EBITA margin of 9.5% and operating cash flow of
EUR 558 million
Amsterdam, July 20, 2020
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Sales amounted to EUR 4.4 billion, with a 6% comparable sales
decrease
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Comparable order intake increased 27%
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Income from continuing operations was EUR 213 million, compared to
EUR 260 million in Q2 2019
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Adjusted EBITA margin was 9.5% of sales, compared to 11.8% of sales
in Q2 2019
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Income from operations amounted to EUR 229 million, compared to EUR
350 million in Q2 2019
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EPS from continuing operations (diluted) amounted to EUR 0.23;
Adjusted EPS amounted to EUR 0.35, compared to EUR 0.42 in Q2
2019
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Operating cash flow improved to EUR 558 million, compared to EUR
390 million in Q2 2019
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Free cash flow increased to EUR 311 million, compared to EUR 174
million in Q2 2019
Frans van Houten, CEO
“As the global societal and economic impact of the COVID-19
outbreak intensified in the second quarter of 2020, we continued to
focus on our triple duty of care: meeting critical customer needs,
safeguarding the health and safety of our employees, and ensuring
business continuity. In close collaboration with our suppliers and
partners, we have steeply ramped up the production volumes of acute
care products and solutions to help diagnose, treat, monitor and
manage COVID-19 patients. Our field service engineers have been
supporting healthcare providers around the world throughout these
testing times. Under the circumstances, I am pleased at the way we
have performed and I am grateful and proud of how all our employees
have stepped up.
In the quarter, Philips' sales declined 6% on a comparable basis
and we delivered an Adjusted EBITA margin of 9.5%. Comparable order
intake grew a further 27% on the back of double-digit growth in the
previous quarter, driven by CT imaging systems, hospital
ventilators and patient monitors. As anticipated, COVID-19 caused a
steep decrease in consumer demand and postponement of installations
in hospitals, as well as elective procedures, resulting in a 19%
comparable sales decrease for our Personal Health businesses and a
9% decline for our Diagnosis & Treatment businesses. This was
partly offset by a strong 14% comparable sales growth for our
Connected Care businesses.
We expect to return to growth and improved profitability for the
Group in the second half of the year, assuming we can convert our
existing order book for the Diagnosis & Treatment and Connected
Care businesses, elective procedures normalize, and consumer demand
gradually improves. Consequently, for the full year 2020 we
continue to aim for a modest comparable sales growth and Adjusted
EBITA margin improvement.
Looking ahead, our mission is more relevant than ever. Our strategy
to transform the delivery of care along the health continuum,
leveraging informatics and remote care capabilities, along with our
innovative systems and services, has been validated during this
crisis. I am convinced that Philips is well positioned to serve the
current and future needs of hospitals and health systems.”
Business segment performance
The Diagnosis & Treatment businesses recorded a 9% comparable
sales decline due to the postponement of installations and elective
procedures. Although Diagnostic Imaging sales were in line with Q2
2019, Ultrasound showed a mid-single-digit decrease, and
Image-Guided Therapy a double-digit decline. Comparable order
intake showed a double-digit decrease. The Adjusted EBITA margin
decreased to 8.6%, mainly due to the sales decline.
Comparable sales in the Connected Care businesses increased 14%,
with double-digit growth in Sleep & Respiratory Care and
mid-single-digit growth in Monitoring & Analytics. Comparable
order intake more than doubled, driven by strong demand for patient
monitors and hospital ventilators. The Adjusted EBITA margin
increased to 17.8%, as additional investments to ramp up production
were more than offset by operating leverage.
The Personal Health businesses recorded a comparable sales decline
of 19%, with all businesses declining due to significantly
decreased consumer demand. The Adjusted EBITA margin declined to
5.6%, due to the sales decline, partly offset by cost savings.
Philips’ ongoing focus on innovation and partnerships resulted in
the following key developments in the quarter:
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Highlighting its strength in strategic partnerships to enhance
patient care and improve care provider productivity, Philips signed
14 new agreements in the quarter. For example, Philips and the US
Department of Veterans Affairs entered a 10-year agreement to
expand their tele-critical care program, creating the world’s
largest system to provide veterans with remote access to intensive
care expertise, regardless of their location. In the Netherlands,
Philips and Flevo Hospital signed a 10-year strategic partnership
agreement to support precision diagnosis and optimize workflows and
patient pathways, while driving efficiencies and cost
optimization.
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In collaboration with its partners and suppliers, Philips tripled
the production of its hospital ventilators in the quarter and is on
track to achieve the planned four-fold increase to 4,000 units per
week in July 2020, supporting the treatment of COVID-19 patients in
the most affected regions around the world.
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Philips launched several new monitoring solutions for the Intensive
Care Unit (ICU), the general ward and the home that feature remote
monitoring capabilities and advanced analytics. These include
Philips’ IntelliVue Patient Monitors MX750/MX850 for the ICU,
Philips’ Biosensor BX100 for early patient deterioration detection
in the general ward, and in collaboration with BioIntelliSense, the
BioSticker medical device to help monitor at-risk patients from the
hospital to the home.
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University of Kentucky HealthCare teamed up with Philips to
implement the company’s tele-ICU technology to enhance patient care
and improve utilization and patient flows across 160 ICU beds at
the academic medical center’s two hospitals. Leveraging Philips’
acute telehealth platform, eCareManager, UK HealthCare is
implementing the state’s first centralized virtual care model to
help nurses detect risk of patient deterioration, so they can
intervene earlier and help improve care outcomes.
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Philips received an industry-first 510(k) clearance from the FDA to
market a wide range of its ultrasound solutions – including CX50
and Lumify – for the management of COVID-19-related lung and
cardiac complications. Portable ultrasound solutions in particular
have become valuable tools for clinicians treating COVID-19
patients, due to their imaging capabilities, portability and ease
of disinfection.
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Supporting the increased demand for flexible ICU capacity, Philips
introduced its new mobile ICUs in India. The ICUs can be furnished
with a range of medical equipment, including ventilators,
defibrillators, and patient monitoring. In the Philippines, Philips
introduced a modular diagnostic imaging cabin with a CT or
diagnostic X-ray system for rapid deployment.
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Complementing Philips Sonicare’s existing teledentistry services
for patients, Philips and dental technology company Toothpic
announced a new teledentistry platform for dental professionals.
The multi-service platform provides a tool to build direct patient
engagement, acquisition and retention while improving office
efficiency, in-chair time and remote care.
Cost savings
In the second quarter, procurement savings amounted to EUR 57
million. Overhead and other productivity programs delivered savings
of EUR 51 million. As a result, Philips is on track to deliver over
EUR 400 million productivity savings for 2020 and EUR 1.8 billion
productivity savings for the Group for the 2017-2020
period.
Executive Committee update
On July 16, Philips announced the appointment of Deeptha Khanna as
the Chief Business Leader of the Personal Health businesses,
effective July 20, 2020, and the appointment of Edwin Paalvast as
Chief of International Markets, effective August 1, 2020. Ms.
Khanna and Mr. Paalvast will become members of Philips’ Executive
Committee, reporting to Philips CEO Frans van Houten.
Ms. Khanna joins Philips from Johnson & Johnson to lead its
Personal Health businesses, which were temporarily led by Frans van
Houten. Mr. Paalvast joins Philips from Cisco Systems, and will
succeed current Chief of International Markets Henk de Jong, who
has been appointed as CEO of Philips’ EUR 2.3 billion Domestic
Appliances business, effective August 1, 2020. As announced in
January 2020, the Domestic Appliances business is being separated
from Philips, a process that is expected to be completed in the
third quarter of 2021. Mr. de Jong will continue to report to Frans
van Houten and remain a member of the Executive Committee.
Capital allocation
Share buyback program
At the end of the first quarter of 2020, Philips had completed
50.3% of its EUR 1.5 billion share buyback program for capital
reduction purposes that was announced on January 29, 2019. In line
with the company’s announcement on March 23, 2020, Philips has
executed the second half of the program through individual forward
transactions with settlement dates extending into the second half
of 2021. Further details can be found here.
Share cancellation
In June 2020, Philips completed the cancellation of 3,809,675
shares that were acquired as part of the share buyback program
mentioned above.
Dividend
In July 2020, Philips issued a total number of 18,080,198 new
common shares for settlement of the 2019 dividend. After deduction
of treasury shares, this results in a total number of outstanding
shares of 909,395,209, compared to 909,194,188 shares in 2019
following the settlement of the 2018 dividend.
Regulatory
update
Philips’ Emergency Care and Resuscitation (ECR) business resumed
manufacturing and shipping of external defibrillators for the US,
following notification from the FDA that the injunction prohibiting
those activities has been lifted. Philips continues to comply with
the terms of the Consent Decree, which remains in effect, and
includes ongoing regulatory compliance monitoring and facility
inspections of the ECR business and of Philips’ other patient care
businesses by the FDA. In connection with the ECR portfolio,
Philips received FDA pre-market approval (PMA) for the HeartStart
FR31)
and HeartStart FRx2)
automated external defibrillators (AEDs), and their supporting
accessories, including batteries and pads.
In connection with the COVID-19 pandemic, Philips is working with
the FDA’s Emergency Response and Product Evaluation teams to
provide them with relevant information, such as Philips’ production
ramp-up and availability of acute care products and solutions to
combat COVID-19. Philips has obtained authorizations through the
FDA’s Emergency Use Authorization (EUA) process for the expanded
use of several of its devices during the COVID-19 public health
emergency, including for the Philips IntelliVue Patient Monitors
MX750/MX850 and its IntelliVue Active Displays AD75/AD85. Moreover,
Philips has received FDA 510(k) clearances to market its Biosensor
BX100 for early patient deterioration detection in the general
ward, and to market a wide range of its ultrasound solutions for
the management of COVID-19-related lung and cardiac
complications.
Conference call and audio webcast
Frans van Houten, CEO, and Abhijit Bhattacharya, CFO, will host a
conference call for investors and analysts at 10:00 am CET today to
discuss the results. A live audio webcast of the conference call
will be available on the Philips Investor Relations website and can
be accessed here.