Enabling discovery, safety and production of tomorrow's therapeutics
HBIO Investor Overview
Jim Green, Chairman, President & CEO
Jennifer Cote, CFO and Treasurer
March 19, 2024
Forward-Looking Statements and Non-GAAP Financial Information
Forward-Looking Statements
This document contains forward-looking statements within the meaning of the federal securities laws, including the Private Securities Litigation Reform Act of 1995. Forward-looking statements may be identified by the use of words such as "may," "will," "expect," "plan," "anticipate," "estimate," "intend" and similar expressions or statements that do not relate to historical matters. Forward-looking statements include, but are not limited to, information concerning expected future financial and operational performance including revenues, gross margins, earnings, cash and debt position, growth and the introduction of new products, and the strength of the Company's market position and business model. Forward-looking statements are not guarantees of future performance and involve known and unknown uncertainties, risks, assumptions, and contingencies, many of which are outside the Company's control. Risks and other factors that could cause the Company's actual results to differ materially from those described its forward-looking statements include those described in the "Risk Factors" section of the Company's most recently filed Annual Report on Form 10-K as well as in the Company's other filings with the Securities and Exchange Commission. Forward-looking statements are based on the Company's expectations and assumptions as of the date of this document. Except as required by law, the Company assumes no obligation to update forward-looking statements to reflect any change in expectations, even as new information becomes available.
Management's Use of Non-GAAP Financial Information
This document includes non-GAAP financial information including one or more of adjusted operating income (loss), adjusted net income (loss), adjusted EBITDA, adjusted EBITDA margin, adjusted diluted earnings (loss) per share, and foreign exchange adjusted revenue. We believe that this non-GAAP financial information provides investors with an enhanced understanding of the underlying operations of the business. For the periods presented, these non-GAAP financial measures have excluded certain expenses and income resulting from items that we do not believe are representative of the underlying operations of the business. Items excluded include stock-based compensation, amortization of intangibles related to acquisitions, litigation settlement, restructuring and other costs, gain/loss on equity securities, income taxes and the tax impact of the reconciling items. Management believes that this non-GAAP financial information is important in comparing current results with prior period results and is useful to investors and financial analysts in assessing the Company's operating performance. Non-GAAP historical financial statement information included herein is accompanied by a reconciliation to the nearest corresponding GAAP measure which is included as exhibits below.
With respect to forward-looking measures, we provide an outlook for adjusted EBITDA margin, and net leverage ratio. Many of the items that we exclude from these forward-looking measure calculations are less capable of being controlled or reliably predicted by management. These items could cause the forward-looking measures presented in our outlook statements to vary materially from our reported net income and other GAAP results.
The non-GAAP financial information provided in this presentation should be considered in addition to, not as a substitute for, the financial information provided and presented in accordance with GAAP and may be different than other companies' non-GAAP financial information.
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Most trusted manufacturer / provider of advanced life science tools to the leading academic research institutions, contract research organizations, pharmaceutical and bio-techs in the discovery, production, and safety & regulatory testing of tomorrow's life-saving therapies
CELLULAR & MOLECULAR
Leading provider of the latest
technologies and tools necessary
for research, discovery and
creation of tomorrow's
breakthrough drugs, vaccines
and therapies.
PRE-CLINICAL SYSTEMS
Market leading provider of the recognized gold standard for data acquisition, processing, and regulatory report generation for safety pharmacology and toxicology testing
COMPANY PROFILE
- Global sales footprint, 3 core manufacturing facilities
- Approx. 420 employees, 33 PhD, 54 Masters, 77 Bachelors
- FY'23 Revenue: $112.3M
- FY'23 Adj. EBITDA: $14.6M (13% of rev), up 34% vs PY*
- 35%+ recurring revenues
- Founded 1901, Public Listing Dec. 2000 "NASDAQ: HBIO"
- Headquarters: Greater Boston, MA
BALANCED PORTFOLIO | ||||
Biotech/ | APAC | |||
25% | ||||
Pharma | ||||
17% | 2023 | 2023 | ||
REVENUE BY | Academic / | |||
REVENUE BY | Americas | |||
CUSTOMER | Research | GEOGRAPHY | ||
TYPE | 45% | |||
CRO / | 51% | |||
Government | EMEA |
30% | |
32% | |
Revenues allocations are approximate |
* Non-GAAP measure; reconciliation to GAAP financial measures are available in Appendix.
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Harvard Bioscience Highlights
Essential, secular growth markets, high | Growing global marquee | |
barriers, few competitors | customer base | |
Global sales, application science and | Highly effective sales channel |
supported by elite | |
service structure | |
applications scientists | |
Technology leadership competitive advantage | High barrier |
with high barrier innovative technologies | innovative technologies |
Robust pipeline of next-gen solutions | Strong discipline, |
lean operating platform | |
DIVERSIFIED CUSTOMER /
REVENUE MODEL
Systems & Software
Consumables
Services
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Sales and Earnings Trends
Expect weakness in the H1 of 2024 vs a strong 2023 comparison; Strong H2 2024 growth vs both H1 2024 and H2 2023
REVENUES
Portfolio Optimization | Flat to Modest | ||
$119M | **** | ||
Revenue Growth** | |||
$113M | $112M | ||
H2H2***
H1H1***
ADJUSTED EBITDA & EBITDA MARGINS*
Adj EBITDA
Margins to the
Mid-Teens**
$18M | $15M | |
15% | $11M | 13% |
10% |
- Non-GAAPmeasure; reconciliations to GAAP financial measures are available in Appendix.
- FY24 Guidance as discussed in Q4 earnings release on March 7, 2024. This presentation is not a reaffirmation of guidance.
- 2024 H1/H2 is approximate for illustrative purposes.
- 2022 Revenue includes $5.5 million in sales of discontinued products; 2023 Revenue includes estimated $0.5 million in sales of discontinued products; net difference is $5.0 million
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Today's Global Footprint
PRE- | ||||
CLINICAL | ||||
SYSTEMS | CELLULAR & | |||
Minneapolis | ||||
MOLECULAR | ||||
AND HBIO | ||||
HEADQUARTERS | ||||
Boston |
Core Operating Site
Sales Office / Small Centers of Excellence
*Headcount is approximate
CELLULAR &
MOLECULAR
Stuttgart, Germany
12-31-18 | 12-31-23 | |
Employees* | 547 | 420 |
Sites | 14 | 8 |
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Essential Technologies Serving Well-funded,High-growth Secular Markets Demographic Tailwinds
DRIVERS
Rising incidence of disease - cardiac, cancer, respiratory, diabetes, obesity, Alzheimer's,
neurological, infectious
Increased funding for research and development of advanced therapeutics
Increased demand for research tools, devices and systems that improve efficiency & productivity and enable therapeutics discovery and safety & regulatory through bio-production
END MARKET | PHARMACEUTICAL1 | BIOTECH2 | CONTRACT RESEARCH | ACADEMIC RESEARCH4 |
ORGANIZATIONS3 | ||||
SEGMENTS | ||||
Estimated | Global | Global | Global | US Federal |
size & | $1.6T 2022 | $372B 2021 | $61B 2021 | $179B 2021 |
projected | 7.7% 2022-2026 | 15.5% 2022-2030 | 10.9% 2021-2030 | 9.3% 2016-2021 |
CAGR | ||||
Pre- | NIH Grants | |||
Estimated R&D | R&D | R&D | clinical | |
expenditure within | $222B | $60B | market | $30.2B |
HBIO markets | (2021)* | (2021)* | $5B | (2021)* |
(2021)5 |
- https://www.researchandmarkets.com/reports/5553406/pharmaceuticals-global-market-report-2022-by
- https://www.acumenresearchandconsulting.com/biotechnology-market
- https://www.emergenresearch.com/request-sample/1221
- https://ncses.nsf.gov/pubs/nsf22323
- https://www.grandviewresearch.com/industry-analysis/preclinical-cro-market
*Internal estimates calculated based on publicly-available data. | 7 |
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Blue Chip Customer Base
ACADEMIC
RESEARCH
- Scientific Research labs primarily government & grant funded
- Early discovery of new novel drugs and compounds for therapies and vaccines
- Advanced cellular testing & gene editing
CONTRACT
RESEARCH
ORGANIZATIONS
- Pre-clinicalstudies to determine safety and efficacy of new pharmaceuticals
- Pharmaceutical companies are outsourcing significant pre-clinical activities to CROs
BIOTECH,
PHARMACEUTICAL
- Perform early discovery and then transition from discovery through pre- clinical regulatory and on to production
- Leverage discoveries from academics & bio-techs
- Bridge to bio-production
Value Proposition | ||
Breakthrough technologies and applications, | Reduce test cycle-time, increase volume and | Reduce development cycle time means more |
increase innovative publications | study types, drives CROs revenue growth | compounds drives BioPharma revenue growth |
Subset of blue-chip recurring customers |
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Extend Technology Leadership in Academic Research & Discovery
Research & Discovery | Pre-Clinical Safety & Toxicology | Bio-Production |
MOLECULES | CELLS | ORGANOIDS/ | PRECLINICAL | CLINICAL |
ORGANS | ||||
Adapt Technologies to High Volume CRO & Bioproduction Applications
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Strategic Growth Drivers
ACCELERATING REVENUE GROWTH
STRENGTHEN THE BASE
- Fortify leadership position and expand recurring revenue in therapy research and pre-clinical testing
- Pre-clinicalTelemetry and GLP
compliant Ponemah data management software for data reporting and analysis
- Electroporation/Transfection/ Amino Acid Analysis
- Micro-ElectrodeArrays (MEAs) cellular electrophysiology
EXPAND HIGH VOLUME APPS
- Offerings for higher volume industrial customers including CROs, Biotech, Pharma and Government Labs
- Reduce cost and improve cycle time/throughput for therapy testing and development
- Expanded Ponemah functionality combined with
new VivaMARS system opens door to new pre-clinical opportunities
EXPAND TO BIO-PRODUCTION
- Offerings for Biotech and Pharma customers engaged in therapy development and production
- Bridge from research to production in applications that scale with production volume
- Leverage technology leadership in Electroporation/Transfection
INNOVATE CELLULAR
- Offerings for Academic, Biotech, and Pharma customers engaged in therapy discovery, development and testing.
- New opportunities for streamlined in vitro testing from cell lines to organoids early in the therapy development cycle.
- Leverage leadership in Micro-Electrode Arrays (MEAs) & electrophysiology
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Disclaimer
Harvard Apparatus Regenerative Technology Inc. published this content on 18 March 2024 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 18 March 2024 21:46:38 UTC.