Thermo Fisher Scientific Reports Fourth Quarter and Full Year 2022 Results

Thermo Fisher Scientific Inc. (NYSE: TMO), the world leader in serving science, today reported its financial results for the fourth quarter and full year ended December 31, 2022.

Fourth Quarter and Full Year 2022 Highlights

  • Fourth quarter revenue grew 7% to $11.45 billion.
  • Fourth quarter GAAP diluted earnings per share (EPS) was $4.01.
  • Fourth quarter adjusted EPS was $5.40.
  • Full year revenue grew 15% to $44.92 billion.
  • Full year GAAP diluted EPS was $17.63.
  • Full year adjusted EPS was $23.24.
  • During the year, we strengthened our industry leadership, advanced our trusted partner status with our customers, delivered excellent financial performance for our shareholders, and invested in our world class team.
  • Achieved outstanding and differentiated Core organic revenue growth, growing 14% in both the fourth quarter and for the full year.
  • Continued to strengthen our unique customer value proposition by adding capacity and capabilities globally for pharma services, bioproduction, and clinical research services. During the fourth quarter, this included the opening of a new state-of-the-art bioanalytical lab in Richmond, Virginia , to support our clinical research business and the increasing demand for analytical services to accelerate drug development.
  • Advanced our industry-leading scale and depth of capabilities in high-growth and emerging markets. During the fourth quarter, this included opening a new biologics manufacturing facility in Hangzhou, China , to offer integrated clinical and commercial drug substance and drug product capabilities for customers.
  • Very active year advancing our environmental, social and governance (ESG) priorities. We made strong progress on our Scope 1 and Scope 2 emissions initiatives, enabling us to increase our 2030 greenhouse gas emissions reduction target and accelerate our transition to 100% renewable energy. Among the highlights from our Foundation for Science, we supported students across the globe through our STEM education programs and colleague-led Community Action Councils. Throughout the year, the company also received a variety of awards and recognition for its industry leadership and inclusive culture including being recognized by Forbes magazine during the quarter as one of the World's Top Female-Friendly Companies and one of America's Best Employers for veterans.
  • Continued to successfully execute our capital deployment strategy in 2022. The integration of PPD is largely complete and drove strong returns for our shareholders with outstanding execution and business performance throughout the year. For the full year, PPD delivered outstanding Core organic revenue growth and is on track to deliver total synergies of $175 million by year 3. Additionally, we returned $3.5 billion of capital to shareholders through stock buybacks and dividends. Shortly after year end, we completed the acquisition of The Binding Site for $2.7 billion.

"We had another exceptional year, exceeding our goals and delivering for all of our stakeholders in 2022," said Marc N. Casper, chairman, president and chief executive officer of Thermo Fisher Scientific. "Thanks to our incredible global team, we successfully executed our proven growth strategy, effectively navigated the macro-environment, and delivered impressive financial results, as we continued to enable our customers to make the world healthier, cleaner and safer."

Casper added, "We are incredibly well positioned as we enter 2023. Our high-impact innovation and unique customer value proposition continue to drive significant share gain. Our experienced management team, PPI Business System and the benefits of scale, position our company to deliver another outstanding year of value creation for all of our stakeholders and ensure we create an even brighter future."

Fourth Quarter 2022

Revenue for the quarter grew 7% to $11.45 billion in 2022, versus $10.70 billion in 2021. Organic revenue was 3% lower, Core organic revenue growth was 14%, and COVID-19 testing revenue was $0.37 billion.

GAAP Earnings Results

GAAP diluted EPS in the fourth quarter of 2022 was $4.01, versus $4.17 in the same quarter last year. GAAP operating income for the fourth quarter of 2022 was $1.86 billion, compared with $2.54 billion in the year-ago quarter. GAAP operating margin was 16.3%, compared with 23.7% in the fourth quarter of 2021.

Non-GAAP Earnings Results

Adjusted EPS in the fourth quarter of 2022 was $5.40, versus $6.54 in the fourth quarter of 2021. Adjusted operating income for the fourth quarter of 2022 was $2.56 billion, compared with $3.16 billion in the year-ago quarter. Adjusted operating margin was 22.4%, compared with 29.5% in the fourth quarter of 2021.

Full Year 2022

Revenue for the full year grew 15% to $44.92 billion in 2022, versus $39.21 billion in 2021. Organic revenue grew slightly, Core organic revenue growth was 14%, and COVID-19 testing revenue was $3.11 billion.

GAAP Earnings Results

GAAP diluted EPS for the full year was $17.63, versus $19.46 in 2021. GAAP operating income for 2022 was $8.39 billion, compared with $10.03 billion a year-ago. GAAP operating margin was 18.7%, compared with 25.6% in 2021.

Non-GAAP Earnings Results

Adjusted EPS for the full year was $23.24, versus $25.13 in 2021. Adjusted operating income for the full year was $10.99 billion, compared with $12.14 billion a year-ago. Adjusted operating margin was 24.5%, compared with 31.0% in 2021.

Annual Guidance for 2023

Thermo Fisher is initiating revenue and adjusted EPS guidance for the full year 2023. The company expects to achieve 2023 revenue of $45.3 billion and full year Core organic revenue growth of 7%. The company expects to achieve adjusted EPS of $23.70.

Use of Non-GAAP Financial Measures

Adjusted EPS, adjusted net income, adjusted operating income, adjusted operating margin, free cash flow, organic revenue growth and Core organic revenue growth are non-GAAP measures that exclude certain items detailed after the tables that accompany this press release, under the heading "Supplemental Information Regarding Non-GAAP Financial Measures." The reconciliations of GAAP to non-GAAP financial measures are provided in the tables that accompany this press release.

Conference Call

Thermo Fisher Scientific will hold its earnings conference call today, February 1, 2023, at 8:30 a.m. Eastern Time. To listen, dial (844) 200-6205 within the U.S. or (929) 526-1599 outside the U.S. The conference ID is 982319. You may also listen to the call live on our website, www.thermofisher.com , by clicking on "Investors." You will find this press release, including the accompanying reconciliation of non-GAAP financial measures and related information, in that section of our website under "Financials." An audio archive of the call will be available under "News & Events" through Friday, February 17, 2023.

About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue over $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com .

Safe Harbor Statement

The following constitutes a "Safe Harbor" statement under the Private Securities Litigation Reform Act of 1995: This press release contains forward-looking statements that involve a number of risks and uncertainties. Important factors that could cause actual results to differ materially from those indicated by forward-looking statements include risks and uncertainties relating to: the duration and severity of the COVID-19 pandemic; the need to develop new products and adapt to significant technological change; implementation of strategies for improving growth; general economic conditions and related uncertainties; dependence on customers' capital spending policies and government funding policies; the effect of economic and political conditions and exchange rate fluctuations on international operations; use and protection of intellectual property; the effect of changes in governmental regulations; any natural disaster, public health crisis or other catastrophic event; and the effect of laws and regulations governing government contracts, as well as the possibility that expected benefits related to recent or pending acquisitions may not materialize as expected. Additional important factors that could cause actual results to differ materially from those indicated by such forward-looking statements are set forth in our most recent annual report on Form 10-K and subsequent quarterly reports on Form 10-Q, which are on file with the SEC and available in the "Investors" section of our website under the heading "SEC Filings." While we may elect to update forward-looking statements at some point in the future, we specifically disclaim any obligation to do so, even if estimates change and, therefore, you should not rely on these forward-looking statements as representing our views as of any date subsequent to today.

Condensed Consolidated Statement of Income (unaudited)

Three Months Ended

December 31,

% of

December 31,

% of

(In millions except per share amounts)

2022

Revenues

2021

Revenues

Revenues

$

11,450

$

10,702

Costs and operating expenses:

Cost of revenues (a)

6,715

58.6

%

5,302

49.5

%

Selling, general and administrative expenses (b)

1,836

16.0

%

1,958

18.3

%

Amortization of acquisition-related intangible assets

592

5.2

%

466

4.4

%

Research and development expenses

391

3.4

%

392

3.7

%

Restructuring and other costs (c)

55

0.5

%

46

0.4

%

9,589

83.7

%

8,164

76.3

%

Operating income

1,861

16.3

%

2,538

23.7

%

Interest income

150

11

Interest expense

(269

)

(161

)

Other income/(expense) (d)

35

(526

)

Income before income taxes

1,777

1,862

Provision for income taxes (e)

(173

)

(202

)

Equity in earnings/(losses) of unconsolidated entities

(30

)

(1

)

Net income

1,574

1,659

Less: net income/(losses) attributable to noncontrolling interests and redeemable noncontrolling interest

(2

)

1

Net income attributable to Thermo Fisher Scientific Inc.

$

1,576

13.8

%

$

1,658

15.5

%

Earnings per share attributable to Thermo Fisher Scientific Inc.:

Basic

$

4.03

$

4.20

Diluted

$

4.01

$

4.17

Weighted average shares:

Basic

391

394

Diluted

393

398

Reconciliation of adjusted operating income and adjusted operating margin

GAAP operating income

$

1,861

16.3

%

$

2,538

23.7

%

Cost of revenues adjustments (a)

5

0.0

%

—

0.0

%

Selling, general and administrative expenses adjustments (b)

47

0.4

%

111

1.0

%

Restructuring and other costs (c)

55

0.5

%

46

0.4

%

Amortization of acquisition-related intangible assets

592

5.2

%

466

4.4

%

Adjusted operating income (non-GAAP measure)

$

2,560

22.4

%

$

3,161

29.5

%

Reconciliation of adjusted net income

GAAP net income attributable to Thermo Fisher Scientific Inc.

$

1,576

$

1,658

Cost of revenues adjustments (a)

5

—

Selling, general and administrative expenses adjustments (b)

47

111

Restructuring and other costs (c)

55

46

Amortization of acquisition-related intangible assets

592

466

Other income/expense adjustments (d)

(46

)

532

Provision for income taxes adjustments (e)

(138

)

(213

)

Equity in earnings/losses of unconsolidated entities

30

1

Adjusted net income (non-GAAP measure)

$

2,121

$

2,601

Reconciliation of adjusted earnings per share

GAAP diluted EPS attributable to Thermo Fisher Scientific Inc.

$

4.01

$

4.17

Cost of revenues adjustments (a)

0.01

0.00

Selling, general and administrative expenses adjustments (b)

0.12

0.28

Restructuring and other costs (c)

0.14

0.11

Amortization of acquisition-related intangible assets

1.50

1.17

Other income/expense adjustments (d)

(0.11

)

1.34

Provision for income taxes adjustments (e)

(0.35

)

(0.53

)

Equity in earnings/losses of unconsolidated entities

0.08

0.00

Adjusted EPS (non-GAAP measure)

$

5.40

$

6.54

Reconciliation of free cash flow

GAAP net cash provided by operating activities

$

3,487

$

2,457

Purchases of property, plant and equipment

(550

)

(831

)

Proceeds from sale of property, plant and equipment

6

11

Free cash flow (non-GAAP measure)

$

2,943

$

1,637

Segment data

Three Months Ended

December 31,

% of

December 31,

% of

(In millions)

2022

Revenues

2021

Revenues

Revenues

Life Sciences Solutions

$

3,046

26.6

%

$

4,150

38.8

%

Analytical Instruments

1,878

16.4

%

1,725

16.1

%

Specialty Diagnostics

1,115

9.7

%

1,447

13.5

%

Laboratory Products and Biopharma Services

5,947

51.9

%

4,195

39.2

%

Eliminations

(536

)

-4.6

%

(815

)

-7.6

%

Consolidated revenues

$

11,450

100.0

%

$

10,702

100.0

%

Operating income and operating margin

Life Sciences Solutions

$

1,040

34.1

%

$

1,999

48.2

%

Analytical Instruments

476

25.4

%

381

22.1

%

Specialty Diagnostics

208

18.6

%

297

20.5

%

Laboratory Products and Biopharma Services

836

14.1

%

484

11.5

%

Subtotal reportable segments

2,560

22.4

%

3,161

29.5

%

Cost of revenues adjustments (a)

(5

)

0.0

%

—

0.0

%

Selling, general and administrative expenses adjustments (b)

(47

)

-0.4

%

(111

)

-1.0

%

Restructuring and other costs (c)

(55

)

-0.5

%

(46

)

-0.4

%

Amortization of acquisition-related intangible assets

(592

)

-5.2

%

(466

)

-4.4

%

GAAP operating income

$

1,861

16.3

%

$

2,538

23.7

%

(a) Adjusted results in 2022 exclude charges for inventory write-downs associated with large-scale abandonment of product lines.

(b) Adjusted results in 2022 and 2021 exclude certain third-party expenses, principally transaction/integration costs related to recent acquisitions, charges/credits for changes in estimates of contingent acquisition consideration, and charges associated with product liability litigation.

(c) Adjusted results in 2022 and 2021 exclude restructuring and other costs consisting principally of severance, impairments of long-lived assets, charges/credits for environmental-related matters, abandoned facility, and other expenses of headcount reductions within several businesses and real estate consolidations. Adjusted results in 2022 also exclude $14 of gain on the sale of intellectual property. Adjusted results in 2021 also exclude $22 of charges for compensation due to employees at recently acquired businesses at the date of acquisition.

(d) Adjusted results in 2022 and 2021 exclude net gains/losses on investments. Adjusted results in 2022 also exclude $67 of net gains on derivative instruments to address certain foreign currency risks and $4 of net settlement gains for pension plans. Adjusted results in 2021 also exclude $570 of losses on the early extinguishment of debt and $10 of charges for the amortization of bridge loan commitment fees related to recent acquisitions.

(e) Adjusted provision for income taxes in 2022 and 2021 excludes incremental tax impacts for the reconciling items between GAAP and adjusted net income, incremental tax impacts as a result of tax rate/law changes and the tax impacts from audit settlements.

Note:

Consolidated depreciation expense is $256 and $217 in 2022 and 2021, respectively.

Organic and Core organic revenue growth

Three months ended

December 31, 2022

Revenue growth

7%

Acquisitions

14%

Currency translation

-4%

Organic revenue growth

-3%

COVID-19 testing revenue

-16%

Contribution of PPD to Core organic revenue growth (a)

1%

Core organic revenue growth

14%

(a) Adjustment to include the contribution of PPD to Core organic revenue growth as though the acquisition had occurred on January 1, 2021.

Note:

For more information related to non-GAAP financial measures, refer to the section titled "Supplemental Information Regarding Non-GAAP Financial Measures" of this release.

Condensed Consolidated Statement of Income (unaudited)

Year ended

December 31,

% of

December 31,

% of

(In millions except per share amounts)

2022

Revenues

2021

Revenues

Revenues

$

44,915

$

39,211

Costs and operating expenses:

Cost of revenues (a)

25,415

56.6

%

18,977

48.4

%

Selling, general and administrative expenses (b)

7,127

15.9

%

6,842

17.4

%

Amortization of acquisition-related intangible assets

2,395

5.3

%

1,761

4.5

%

Research and development expenses

1,471

3.3

%

1,406

3.6

%

Restructuring and other costs (c)

114

0.3

%

197

0.5

%

36,522

81.3

%

29,183

74.4

%

Operating income

8,393

18.7

%

10,028

25.6

%

Interest income

272

43

Interest expense

(726

)

(536

)

Other income/(expense) (d)

(104

)

(694

)

Income before income taxes

7,835

8,841

Provision for income taxes (e)

(703

)

(1,109

)

Equity in earnings/(losses) of unconsolidated entities

(172

)

(4

)

Net income

6,960

7,728

Less: net income/(losses) attributable to noncontrolling interests and redeemable noncontrolling interest

10

3

Net income attributable to Thermo Fisher Scientific Inc.

$

6,950

15.5

%

$

7,725

19.7

%

Earnings per share attributable to Thermo Fisher Scientific Inc.:

Basic

$

17.75

$

19.62

Diluted

$

17.63

$

19.46

Weighted average shares:

Basic

392

394

Diluted

394

397

Reconciliation of adjusted operating income and adjusted operating margin

GAAP operating income

$

8,393

18.7

%

$

10,028

25.6

%

Cost of revenues adjustments (a)

46

0.1

%

8

0.0

%

Selling, general and administrative expenses adjustments (b)

37

0.1

%

144

0.4

%

Restructuring and other costs (c)

114

0.3

%

197

0.5

%

Amortization of acquisition-related intangible assets

2,395

5.3

%

1,761

4.5

%

Adjusted operating income (non-GAAP measure)

$

10,985

24.5

%

$

12,138

31.0

%

Reconciliation of adjusted net income

GAAP net income attributable to Thermo Fisher Scientific Inc.

$

6,950

$

7,725

Cost of revenues adjustments (a)

46

8

Selling, general and administrative expenses adjustments (b)

37

144

Restructuring and other costs (c)

114

197

Amortization of acquisition-related intangible assets

2,395

1,761

Other income/expense adjustments (d)

117

732

Provision for income taxes adjustments (e)

(672

)

(593

)

Equity in earnings/losses of unconsolidated entities

172

4

Adjusted net income (non-GAAP measure)

$

9,159

$

9,978

Reconciliation of adjusted earnings per share

GAAP diluted EPS attributable to Thermo Fisher Scientific Inc.

$

17.63

$

19.46

Cost of revenues adjustments (a)

0.12

0.02

Selling, general and administrative expenses adjustments (b)

0.09

0.36

Restructuring and other costs (c)

0.29

0.50

Amortization of acquisition-related intangible assets

6.07

4.43

Other income/expense adjustments (d)

0.30

1.84

Provision for income taxes adjustments (e)

(1.70

)

(1.49

)

Equity in earnings/losses of unconsolidated entities

0.44

0.01

Adjusted EPS (non-GAAP measure)

$

23.24

$

25.13

Reconciliation of free cash flow

GAAP net cash provided by operating activities

$

9,154

$

9,312

Purchases of property, plant and equipment

(2,243

)

(2,523

)

Proceeds from sale of property, plant and equipment

24

20

Free cash flow (non-GAAP measure)

$

6,935

$

6,809

Segment data

Year ended

December 31,

% of

December 31,

% of

(In millions)

2022

Revenues

2021

Revenues

Revenues

Life Sciences Solutions

$

13,532

30.1

%

$

15,631

39.9

%

Analytical Instruments

6,624

14.7

%

6,069

15.5

%

Specialty Diagnostics

4,763

10.6

%

5,659

14.4

%

Laboratory Products and Biopharma Services

22,511

50.1

%

14,862

37.9

%

Eliminations

(2,515

)

-5.5

%

(3,010

)

-7.7

%

Consolidated revenues

$

44,915

100.0

%

$

39,211

100.0

%

Operating income and operating margin

Life Sciences Solutions

$

5,582

41.2

%

$

7,817

50.0

%

Analytical Instruments

1,507

22.8

%

1,197

19.7

%

Specialty Diagnostics

1,024

21.5

%

1,280

22.6

%

Laboratory Products and Biopharma Services

2,872

12.8

%

1,844

12.4

%

Subtotal reportable segments

10,985

24.5

%

12,138

31.0

%

Cost of revenues adjustments (a)

(46

)

-0.1

%

(8

)

0.0

%

Selling, general and administrative expenses adjustments (b)

(37

)

-0.1

%

(144

)

-0.4

%

Restructuring and other costs (c)

(114

)

-0.3

%

(197

)

-0.5

%

Amortization of acquisition-related intangible assets

(2,395

)

-5.3

%

(1,761

)

-4.5

%

GAAP operating income

$

8,393

18.7

%

$

10,028

25.6

%

(a) Adjusted results in 2022 and 2021 exclude charges for the sale of inventories revalued at the date of acquisition. Adjusted results in 2022 also exclude $27 of inventory write-downs associated with large-scale abandonment of product lines.

(b) Adjusted results in 2022 and 2021 exclude certain third-party expenses, principally transaction/integration costs related to recent acquisitions, charges/credits for changes in estimates of contingent acquisition consideration, and charges associated with product liability litigation.

(c) Adjusted results in 2022 and 2021 exclude restructuring and other costs consisting principally of severance, impairments of long-lived assets, charges/credits for environmental-related matters, abandoned facility and other expenses of headcount reductions within several businesses and real estate consolidations. Adjusted results in 2022 also exclude $14 of gain on the sale of intellectual property. Adjusted results in 2021 also exclude $122 of charges for impairments of acquired intangible assets and $35 of charges for compensation due to employees at recently acquired businesses at the date of acquisition.

(d) Adjusted results in 2022 and 2021 exclude net gains/losses on investments and losses on the early extinguishment of debt. Adjusted results in 2022 also exclude $67 of net gains on derivative instruments to address certain foreign currency risks and $2 of net settlement gains for pension plans. Adjusted results in 2021 also exclude $36 of charges for amortization of bridge loan commitment fees related to a pending acquisition.

(e) Adjusted provision for income taxes in 2022 and 2021 excludes incremental tax impacts for the reconciling items between GAAP and adjusted net income, incremental tax impacts as a result of tax rate/law changes and the tax impacts from audit settlements (including a $658 benefit from an audit settlement in 2022). Adjusted results in 2022 also exclude a $423 charge for the impact of deferred tax realizability assessments as a result of audit settlements.

Notes:

Consolidated depreciation expense is $986 and $831 in 2022 and 2021, respectively.

Organic and Core organic revenue growth

Twelve months ended

December 31, 2022

Revenue growth

15%

Acquisitions

18%

Currency translation

-3%

Organic revenue growth

0%

COVID-19 testing revenue

-13%

Contribution of PPD to Core organic revenue growth (a)

1%

Core organic revenue growth

14%

(a) Adjustment to include the contribution of PPD to Core organic revenue growth as though the acquisition had occurred on January 1, 2021.

Note:

For more information related to non-GAAP financial measures, refer to the section titled "Supplemental Information Regarding Non-GAAP Financial Measures" of this release.

Condensed Consolidated Balance Sheet (unaudited)

December 31,

December 31,

(In millions)

2022

2021

Assets

Current assets:

Cash and cash equivalents

$

8,524

$

4,477

Accounts receivable, net

8,274

7,977

Inventories

5,634

5,051

Other current assets

2,933

2,608

Total current assets

25,365

20,113

Property, plant and equipment, net

9,280

8,333

Acquisition-related intangible assets, net

17,442

20,113

Other assets

4,007

4,640

Goodwill

41,196

41,924

Total assets

$

97,290

$

95,123

Liabilities, redeemable noncontrolling interest and equity

Current liabilities:

Short-term obligations and current maturities of long-term obligations

$

5,579

$

2,537

Other current liabilities

11,535

10,899

Total current liabilities

17,114

13,436

Other long-term liabilities

7,119

8,377

Long-term obligations

28,909

32,333

Redeemable noncontrolling interest

116

122

Total equity

44,032

40,855

Total liabilities, redeemable noncontrolling interest and equity

$

97,290

$

95,123

Condensed Consolidated Statement of Cash Flows (unaudited)

Year ended

December 31,

December 31,

(In millions)

2022

2021

Operating activities

Net income

$

6,960

$

7,728

Adjustments to reconcile net income to net cash provided by operating activities:

Depreciation and amortization

3,381

2,592

Change in deferred income taxes

(995

)

(647

)

Other non-cash expenses, net

857

1,187

Changes in assets and liabilities, excluding the effects of acquisitions

(1,049

)

(1,548

)

Net cash provided by operating activities

9,154

9,312

Investing activities

Acquisitions, net of cash acquired

(39

)

(19,395

)

Purchases of property, plant and equipment

(2,243

)

(2,523

)

Proceeds from sale of property, plant and equipment

24

20

Other investing activities, net

99

(34

)

Net cash used in investing activities

(2,159

)

(21,932

)

Financing activities

Net proceeds from issuance of debt

3,193

18,137

Repayment of debt

(375

)

(11,738

)

Net proceeds from issuance of commercial paper

1,526

2,512

Repayment of commercial paper

(3,690

)

—

Purchases of company common stock

(3,000

)

(2,000

)

Dividends paid

(455

)

(395

)

Other financing activities, net

(9

)

65

Net cash (used in) provided by financing activities

(2,810

)

6,581

Exchange rate effect on cash

(139

)

194

Increase (decrease) in cash, cash equivalents and restricted cash

4,046

(5,845

)

Cash, cash equivalents and restricted cash at beginning of period

4,491

10,336

Cash, cash equivalents and restricted cash at end of period

$

8,537

$

4,491

Free cash flow (non-GAAP measure)

$

6,935

$

6,809

Note:

For more information related to non-GAAP financial measures, refer to the section titled "Supplemental Information Regarding Non-GAAP Financial Measures" of this release.

Supplemental Information Regarding Non-GAAP Financial Measures

In addition to the financial measures prepared in accordance with generally accepted accounting principles (GAAP), we use certain non-GAAP financial measures such as organic revenue growth, which is reported revenue growth, excluding the impacts of revenues from acquired businesses and the effects of currency translation. We also report Core organic revenue growth, which is reported revenue growth including the impact of PPD revenue, excluding the impacts of COVID-19 testing revenue, and excluding the impacts of acquisitions other than PPD and currency translation. We calculate period-to-period Core organic revenue growth by adding to the baseline period PPD's pre-acquisition revenues from such period. We report these measures because Thermo Fisher management believes that in order to understand the company's short-term and long-term financial trends, investors may wish to consider the impact of acquisitions, foreign currency translation and/or COVID-19 testing on revenues. In particular, given PPD's significance relative to our existing businesses, management believes it is appropriate to also present information on a basis that includes PPD pre-acquisition revenues in order to demonstrate the impact PPD has on our current growth profile. Core organic revenue growth amounts are not necessarily indicative of the combined results of operations that would have been realized had the PPD acquisition occurred on January 1, 2021. Thermo Fisher management uses these measures to forecast and evaluate the operational performance of the company as well as to compare revenues of current periods to prior periods.

We report adjusted operating income, adjusted operating income margin, adjusted net income, and adjusted EPS. We believe that the use of these non-GAAP financial measures, in addition to GAAP financial measures, helps investors to gain a better understanding of our core operating results and future prospects, consistent with how management measures and forecasts the company's core operating performance, especially when comparing such results to previous periods, forecasts, and to the performance of our competitors. Such measures are also used by management in their financial and operating decision-making and for compensation purposes. To calculate these measures we exclude, as applicable:

  • Certain acquisition-related costs, including charges for the sale of inventories revalued at the date of acquisition, significant transaction/acquisition-related costs, including changes in estimates of contingent acquisition-related consideration, and other costs associated with obtaining short-term financing commitments for pending/recent acquisitions. We exclude these costs because we do not believe they are indicative of our normal operating costs.
  • Costs/income associated with restructuring activities and large-scale abandonments of product lines, such as reducing overhead and consolidating facilities. We exclude these costs because we believe that the costs related to restructuring activities are not indicative of our normal operating costs.
  • Equity in earnings/losses of unconsolidated entities; impairments of long-lived assets; and certain other gains and losses that are either isolated or cannot be expected to occur again with any predictability, including gains/losses on investments, the sale of businesses, product lines, and real estate, significant litigation-related matters, curtailments/settlements of pension plans, and the early retirement of debt. We exclude these items because they are outside of our normal operations and/or, in certain cases, are difficult to forecast accurately for future periods.
  • The expense associated with the amortization of acquisition-related intangible assets because a significant portion of the purchase price for acquisitions may be allocated to intangible assets that have lives of up to 20 years. Exclusion of the amortization expense allows comparisons of operating results that are consistent over time for both our newly acquired and long-held businesses and with both acquisitive and non-acquisitive peer companies.
  • The tax impacts of the above items and the impact of significant tax audits or events (such as changes in deferred taxes from enacted tax rate/law changes), the latter of which we exclude because they are outside of our normal operations and difficult to forecast accurately for future periods.

We report free cash flow, which is operating cash flow excluding net capital expenditures, to provide a view of the continuing operations' ability to generate cash for use in acquisitions and other investing and financing activities. The company also uses this measure as an indication of the strength of the company. Free cash flow is not a measure of cash available for discretionary expenditures since we have certain non-discretionary obligations such as debt service that are not deducted from the measure.

Thermo Fisher Scientific does not provide GAAP financial measures on a forward-looking basis because we are unable to predict with reasonable certainty and without unreasonable effort items such as the timing and amount of future restructuring actions and acquisition-related charges as well as gains or losses from sales of real estate and businesses, the early retirement of debt and the outcome of legal proceedings. The timing and amount of these items are uncertain and could be material to Thermo Fisher Scientific's results computed in accordance with GAAP.

The non-GAAP financial measures of Thermo Fisher Scientific's results of operations and cash flows included in this press release are not meant to be considered superior to or a substitute for Thermo Fisher Scientific's results of operations prepared in accordance with GAAP. Reconciliations of such non-GAAP financial measures to the most directly comparable GAAP financial measures are set forth in the tables above.

Media Contact Information:
Sandy Pound
Thermo Fisher Scientific
Phone: 781-622-1223
E-mail: sandy.pound@thermofisher.com

Investor Contact Information:
Rafael Tejada
Thermo Fisher Scientific
Phone: 781-622-1356
E-mail: rafael.tejada@thermofisher.com

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Medtronic to announce financial results for its fourth quarter and full fiscal year 2025

Medtronic to announce financial results for its fourth quarter and full fiscal year 2025

- Medtronic plc (NYSE: MDT), a global leader in healthcare technology, today announced that it will report financial results for its fourth quarter and full fiscal year 2025 on Wednesday, May 21, 2025 . A news release will be issued at approximately 5:45 a.m. Central Daylight Time (CDT) and will be available at https:news.medtronic.com . The news release will include summary financial information for the company's fourth quarter and full fiscal year 2025, which ended on Friday, April 25, 2025 .

Medtronic will host a video webcast at 7:00 a.m. CDT on May 21, 2025 , to discuss results for its fourth quarter and full fiscal year 2025. The webcast can be accessed at https://investorrelations.medtronic.com .

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New survey: 1 in 3 women have not talked to their doctor about heart health, the #1 killer of women

Star Jones , award winning television personality & women's heart health advocate,   helps kick off heart health conversations this Mother's Day with the Medtronic 'Letter to My Mother' campaign

A new Medtronic-sponsored survey of women ages 30-50 reveals a significant gap in awareness and discussion around heart health among women and their mother-figures. Despite cardiovascular disease being the #1 killer of women in the U.S. many women are still unaware of the risk and the importance of heart health.

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Medtronic Affera pulsed field ablation technologies continue to demonstrate promising evidence for atrial fibrillation patients

Medtronic Affera pulsed field ablation technologies continue to demonstrate promising evidence for atrial fibrillation patients

  • One-year clinical trial data for the next-generation, investigational, Sphere-360â„¢ single-shot PFA catheter show impressive safety, performance, and efficiency results for paroxysmal Afib
  • Dual-energy (RF/PF), focal Sphere-9â„¢ catheter demonstrates efficacy for linear ablation in persistent AFib
  • Medtronic continues legacy of leadership in innovation, showcasing arrhythmia management portfolio at Heart Rhythm Society annual meeting

Medtronic plc (NYSE: MDT), a global leader in healthcare technology, today announced positive clinical outcomes from two studies in atrial fibrillation (AFib) patients treated with the Afferaâ„¢ family of technologies, including the next-generation Sphere-360â„¢ single-shot pulsed field ablation (PFA) catheter and the groundbreaking Sphere-9â„¢ combination mapping and dual-energy focal PFA catheter. Data were presented in High Impact Science Sessions at the Heart Rhythm Society 2025 Annual Meeting in San Diego ; the Sphere-360 study was simultaneously published in the Heart Rhythm Journal .

(PRNewsfoto/Medtronic plc)

Sphere-360 Study Safety and Performance

Sphere-360 is an investigational, first-of-its-kind, single-shot PFA mapping and ablation catheter for treatment of paroxysmal atrial fibrillation (PAF). Results for Sphere-360 at one year, in a prospective, single-arm, multi-center trial performed in European centers, demonstrated freedom from arrhythmia recurrence in 88% of patients, with chronically durable pulmonary vein isolation (PVI) in 98% of targeted veins and no reported safety events in a sub-group treated with the most optimized waveform. The Sphere-360 catheter has a large, conformable lattice design that can be modified into various shapes, is seamlessly integrated with the Affera Mapping and Ablation System and utilizes an 8.5 Fr sheath – the smallest in any single-shot PFA technology.

"The Affera technology is a sophisticated ecosystem, including an advanced, intuitive mapping system and catheters that are seamlessly integrated to offer treatment options for different cardiac arrhythmias. It is encouraging to see the promising results for Sphere-360, which can easily create circumferential lesions without the need for catheter rotation," said Vivek Reddy , M.D., Director of Cardiac Arrhythmia Services for the Mount Sinai Health System in New York City . "The study results showed Sphere-360 has a promising safety and performance profile with zero serious adverse events observed. Upon approval, Sphere-360 will be a valuable addition to Medtronic's Affera system, which has been a game changer for Afib treatment and physician workflow."

Medtronic intends to begin its U.S. pivotal trial for the Sphere-360 catheter later this calendar year. Worldwide, Sphere-360 is currently investigational and not approved for sale or distribution.

Sphere-9 for Linear Ablation

Additionally, in a sub-analysis from the Sphere Per-AF IDE study , results demonstrated that the Sphere-9 catheter can be used safely and effectively to create linear lesions in persistent AF patients. Linear ablation is often used in conjunction with PVI to improve the chances of restoring a normal heart rhythm without recurrence in persistent AF patients. The Sphere Per-AF IDE study evaluated the safety, efficacy and efficiency of Affera and Sphere-9 in persistent AF and led to the FDA approval of Affera in October 2024 .

"True to our Medtronic mission for patients and legacy of innovation, we are delivering our best-in-class technologies to physicians and improving care for AFib patients, and we are not slowing down," said Rebecca Seidel , president of the Cardiac Ablation Solutions business at Medtronic, which is part of the Cardiovascular portfolio. "These results signify another step forward and energize us as we continue to earn and build our leadership position in electrophysiology every day."

Medtronic is the only company with two PFA offerings for physicians and patients. The PulseSelectâ„¢ Pulsed Field Ablation System offers physicians a safe, single-shot solution for pulmonary vein isolation (PVI) and is now available in more than 30 countries. The Affera system together with the Sphere-9 catheter enables physician treatment flexibility with its wide area focal design and 9mm lattice tip that can used with an 8.5Fr sheath. Affera is available in Europe , Australia and New Zealand , with global expansion ongoing.

AFib is one of the most common and undertreated heart rhythm disorders, affecting more than 60 million people worldwide. 1 Afib is a progressive disease, often beginning as paroxysmal AFib (presents intermittently) and progressing to persistent (lasts for more than 7+ days without stopping). As the disease progresses, the risk of serious complications including heart failure, stroke and risk of death increases 2-5 .

For more information on the Affera PFA system and the Sphere-9 catheter, visit Medtronic.com.

About Medtronic

Bold thinking. Bolder actions. We are Medtronic. Medtronic plc, headquartered in Galway , Ireland , is the leading global healthcare technology company that boldly attacks the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people across more than 150 countries. Our technologies and therapies treat 70 health conditions and include cardiac devices, surgical robotics, insulin pumps, surgical tools, patient monitoring systems, and more. Powered by our diverse knowledge, insatiable curiosity, and desire to help all those who need it, we deliver innovative technologies that transform the lives of two people every second, every hour, every day. Expect more from us as we empower insight-driven care, experiences that put people first, and better outcomes for our world. In everything we do, we are engineering the extraordinary. For more information on Medtronic (NYSE: MDT), visit www.Medtronic.com and follow Medtronic on LinkedIn .

Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's periodic reports on file with the Securities and Exchange Commission. Actual results may differ materially from anticipated results.

References

  1. Roth GA, Mensah GA, Johnson CO et al. Global Burden of Cardiovascular Diseases and Risk Factors, 1990-2019: Update From the GBD 2019 Study. J Am Coll Cardiol 2020;76:2982-3021.
  2. Miyasaka Y, Barnes ME, Bailey KR, et al. Mortality trends in patients diagnosed with first atrial fibrillation: a 21-year community-based study. J Am Coll Cardiol 2007;49:986-92.
  3. Hindricks G, Potpara T, Dagres N, et al. 2020 ESC Guidelines for the diagnosis and management of atrial fibrillation developed in collaboration with the European Association of Cardio-Thoracic Surgery (EACTS). Eur Heart J 2020.
  4. Wolf PA , Abbott RD, Kannel WB. Atrial fibrillation as an independent risk factor for stroke: the Framingham Study. Stroke 1991;22:983-8.
  5. Lubitz SA, Moser C, Sullivan L, et al. Atrial fibrillation patterns and risks of subsequent stroke, heart failure, or death in the community. J Am Heart Assoc 2013;2:e000126

Dr. Reddy is a paid consultant for Medtronic.

Contacts:
Leslie Williamson
Public Relations
+1-612-227-5099

Ryan Weispfenning
Investor Relations
+1-763-505-4626

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SOURCE Medtronic plc

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Largest multi-center prospective Investigational Device Exemption (IDE) study for multi-port robotic-assisted urologic surgery   in the U.S. presented as a late-breaker at the American Urologic Association annual meeting

Company confirms Hugo RAS system submission to the U.S. Food and Drug Administration

Medtronic (NYSE: MDT), a global leader in healthcare technology, today announced that the Expand URO Investigational Device Exemption (IDE) clinical study, the largest such study for robotic-assisted urologic surgery ever conducted, met both primary safety and effectiveness endpoints. The prospective, multi-center, single-arm IDE study included 137 patients who underwent urologic procedures using the Hugoâ„¢ robotic-assisted surgery (RAS) system.

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Adding to the Medtronic portfolio of catheter-based lead solutions, the novel OmniaSecure defibrillation lead allows for precise delivery and placement in the right ventricle

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Medtronic plc (NYSE: MDT), a global leader in healthcare technology, today announced it has submitted 510(k) applications to the U.S. Food and Drug Administration (FDA) seeking clearance for an interoperable pump. FDA clearance of this pump would pave the way for system integration with a continuous glucose monitoring (CGM) sensor based on Abbott's most advanced CGM platform.

(PRNewsfoto/Medtronic plc)

The submissions included a 510(k) application for its MiniMedâ„¢ 780G pump as an alternate controller enabled (ACE) insulin pump and a separate 510(k) application for its SmartGuardâ„¢ algorithm as an interoperable automated glycemic controller (iAGC).

"We understand how meaningful these advancements are, and we're working with urgency to bring enhanced CGM options to our customers," said Que Dallara, EVP & president, Medtronic Diabetes. "This collaboration with Abbott marks an important step forward in providing innovative solutions and more choice for our customers."

This milestone follows the announcement last August that the companies will collaborate on an integrated system based on Abbott's most advanced CGM platform. Abbott will supply Medtronic with a CGM that will work exclusively with Medtronic smart dosing devices and software across both automated insulin delivery and smart multiple daily injections systems. These systems, including the Abbott CGM, will be sold exclusively by Medtronic.

More details will be shared when FDA clearance is secured.

About the Diabetes Business at Medtronic ( www.medtronicdiabetes.com )
Medtronic Diabetes is on a mission to alleviate the burden of diabetes by empowering individuals to live life on their terms, with the most advanced diabetes technology and always-on support when and how they need it. We've pioneered first-of-its-kind innovations for over 40 years and are committed to designing the future of diabetes management through next-generation sensors (CGM), intelligent dosing systems, and the power of data science and AI while always putting the customer experience at the forefront.

About Medtronic
Bold thinking. Bolder actions. We are Medtronic. Medtronic plc, headquartered in Galway , Ireland , is the leading global healthcare technology company that boldly attacks the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people across more than 150 countries. Our technologies and therapies treat 70 health conditions and include cardiac devices, surgical robotics, insulin pumps, surgical tools, patient monitoring systems, and more. Powered by our diverse knowledge, insatiable curiosity, and desire to help all those who need it, we deliver innovative technologies that transform the lives of two people every second, every hour, every day. Expect more from us as we empower insight-driven care, experiences that put people first, and better outcomes for our world. In everything we do, we are engineering the extraordinary. For more information on Medtronic (NYSE: MDT), visit www.Medtronic.com and follow Medtronic on LinkedIn .

Any forward-looking statements, including, but not limited to, statements regarding the partnership between Medtronic and Abbott, strategic and other potential benefits of the partnership, Abbott's products and product candidates, and other statements about Medtronic managements' future expectations, beliefs, goals, plans or prospects, are subject to risks and uncertainties including, but not limited to, the ability to obtain regulatory approvals, and other risks and uncertainties such as those described in Medtronic's reports and other filings with the Securities and Exchange Commission. Actual results may differ materially from anticipated results. Medtronic cautions investors not to place considerable reliance on the forward-looking statements contained in this press release. These forward-looking statements speak only as of the date of this document, and Medtronic undertakes no obligation to update or revise any of these statements except to the extent required by law.

Contacts:
Janet Cho
Public Relations
+1-818-403-7028

Ryan Weispfenning
Investor Relations
+1-763-505-4626

View original content to download multimedia: https://www.prnewswire.com/news-releases/medtronic-advances-abbott-cgm-partnership-with-fda-submission-of-interoperable-insulin-pump-302437337.html

SOURCE Medtronic plc

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