Inotiv, Inc. (NOTV): History, Ownership, Mission, How It Works & Makes Money

Inotiv, Inc. (NOTV): History, Ownership, Mission, How It Works & Makes Money

US | Healthcare | Medical - Diagnostics & Research | NASDAQ

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As a seasoned financial analyst, I'm looking at Inotiv, Inc. (NOTV) and asking: can this contract research organization (CRO) truly accelerate drug discovery while navigating its own operational headwinds?

The company, which specializes in nonclinical and analytical drug development services, is projecting full fiscal year 2025 revenue between $512.5 million and $513.5 million, a modest increase over the prior year, but its core Discovery and Safety Assessment (DSA) segment is showing huge momentum, with contract awards up 60% year-over-year in the fourth quarter.

Still, you have to weigh that against a market capitalization of just over $29 million and a recent stock price of around $0.83 per share, which signals significant investor skepticism; so, what does this disconnect tell you about the real value proposition of their mission to bring new drugs to market?

We'll break down the history, the BlackRock, Inc. and institutional ownership structure, and the mechanics of how Inotiv makes money, giving you the precise data needed to make your own informed decision.

Inotiv, Inc. (NOTV) History

Inotiv, Inc. is a contract research organization (CRO) with roots stretching back over five decades, built on a foundation of analytical instrumentation before evolving into a comprehensive drug discovery and development services provider. The company's modern identity is the result of strategic mergers and acquisitions, most notably the 2018 combination of Bioanalytical Systems, Inc. (BASi) and Seventh Wave Laboratories, which set the stage for the Inotiv brand.

Given Company's Founding Timeline

Year established

The company was originally established in 1974 as Bioanalytical Systems, Inc. (BASi).

Original location

West Lafayette, Indiana, where it was launched as a resource for research laboratories.

Founding team members

The original founder was Dr. Peter Kissinger, a chemistry professor at Purdue University, who launched BASi.

Initial capital/funding

Specific initial capital details are not publicly available, but the company's early focus was on selling analytical instruments and consumables to research labs. For a sense of their later financing, a December 2024 equity offering raised net proceeds of approximately $24.0 million, a crucial liquidity injection for the 2025 fiscal year.

Given Company's Evolution Milestones

The company's history is a clear map of expanding its service offerings through strategic acquisitions, moving from selling instruments to providing full-service nonclinical and analytical drug development support.

Year Key Event Significance
1974 Bioanalytical Systems, Inc. (BASi) is founded. Established the foundational business in scientific instrumentation and consumables for research.
1997 Initial Public Offering (IPO). Transitioned into a publicly traded company on the Nasdaq Stock Market.
2018 BASi merges with Seventh Wave Laboratories. A pivotal move that expanded the company's contract research services and laid the groundwork for the unified Inotiv brand.
2021 (March) Rebranded as Inotiv, Inc. Consolidated various acquired contract research services under a single, unified corporate identity.
2021 (November) Acquisition of Envigo RMS Holding Corp. Significantly expanded the company's scale and capabilities, creating a more comprehensive offering for drug developers.
2022 Divestiture of the Research Model and Services (RMS) business. Simplified the business model, reducing operational complexity to refocus on the higher-growth Discovery and Safety Assessment segments.

Given Company's Transformative Moments

The real inflection points for Inotiv were less about incremental growth and more about massive, strategic shifts in what they actually sell. You're looking at a company that fundamentally changed its business model twice.

  • The Pivot from Product to Service: The merger with Seventh Wave in 2018 and the subsequent rebranding to Inotiv in 2021 signaled a definitive move away from being primarily an instrument manufacturer (BASi) to becoming a full-service Contract Research Organization (CRO). This is defintely the biggest strategic decision.
  • The Envigo Acquisition and Subsequent Streamlining: The November 2021 acquisition of Envigo RMS Holding Corp. was a game-changer, but it also created complexity. The subsequent 2022 divestiture of the RMS business segment for approximately $53.5 million was a crucial cleanup, allowing management to focus resources and capital on the most profitable segments.
  • Navigating 2025 Financial Headwinds: The company's performance in the 2025 fiscal year highlights a focus on stabilization. For instance, the second quarter of fiscal year 2025 saw revenue of $124.3 million, followed by a rise to $130.7 million in the third quarter, showing a sequential revenue improvement despite ongoing market challenges. This demonstrates a leadership team actively steering the ship through a challenging period. For a deeper dive into the numbers, you should read Breaking Down Inotiv, Inc. (NOTV) Financial Health: Key Insights for Investors.

Here's the quick math: the divestiture helped them shed complexity and focus on higher-margin Discovery and Safety Assessment work, which is where the real value is created in the long run.

Inotiv, Inc. (NOTV) Ownership Structure

Inotiv, Inc. (NOTV) is a publicly traded contract research organization, meaning its ownership is distributed among a mix of institutional investors, company insiders, and the general public. This structure ensures a degree of public accountability but also means a significant portion of its shares, almost 40%, are held by parties with a direct stake in the company's long-term operations or professional investment mandates.

Inotiv, Inc.'s Current Status

Inotiv, Inc. is a publicly traded company, listed on the NASDAQ stock exchange under the ticker symbol NOTV. Being public means the company is subject to rigorous reporting requirements from the Securities and Exchange Commission (SEC), which provides you, the investor, with a clear view into its operations and financial health. For the full fiscal year 2025, the company anticipates consolidated revenue to be between $512.5 million and $513.5 million, with the Discovery and Safety Assessment (DSA) services business showing a strong book-to-bill ratio of approximately 1.05x. That's a solid forward indicator for the core business.

Inotiv, Inc.'s Ownership Breakdown

Understanding who owns the stock is crucial because it tells you whose interests are driving the company's strategy. As of November 2025, institutional holders-the big money managers like Vanguard Group Inc. and Balyasny Asset Management L.P.-control a sizable but not dominant share. Insiders, which includes executives and directors, hold a notable stake, which is defintely a good sign for alignment of interests with shareholders.

Shareholder Type Ownership, % Notes
Institutional Investors 25.43% Includes mutual funds, hedge funds, and major asset managers.
Company Insiders 11.3% Held by executives and directors, indicating management's skin in the game.
Retail and Other Public Shareholders 63.27% The remaining shares held by individual investors and smaller funds.

For a deeper dive into which specific funds and institutions are buying and selling, you should check out Exploring Inotiv, Inc. (NOTV) Investor Profile: Who's Buying and Why?

Inotiv, Inc.'s Leadership

The company's direction is steered by a management team focused on executing its contract research organization (CRO) strategy, particularly in the Discovery and Safety Assessment (DSA) and Research Models and Services (RMS) segments. This team has been actively meeting with investors in November 2025 to discuss their performance and outlook.

The key executives leading Inotiv, Inc. as of late 2025 include:

  • Robert Leasure Jr.: Chief Executive Officer, President, and Director. He is the face of the company's strategic vision.
  • Beth A. Taylor: Executive Vice President and Chief Financial Officer (CFO). She manages the financial health, a critical role given the company's debt levels.
  • Greg Beattie: Chief Operating Officer, DSA. He oversees the core Discovery and Safety Assessment services.
  • John Sagartz, DVM, PhD, DACVP: Chief Strategy Officer and Director. His role is to map out the long-term strategic path.
  • Andrea Castetter: Executive Vice President - General Counsel, Corporate Secretary and Chief Compliance Officer. She handles all legal and compliance matters.

The leadership's primary challenge remains balancing growth, especially in DSA services, with managing the company's financial strength, which has been rated as poor due to high debt levels.

Inotiv, Inc. (NOTV) Mission and Values

Inotiv, Inc.'s core purpose transcends pure profit, centering on accelerating the development of life-saving therapeutics by being a trusted scientific partner. This mission is backed by a clear vision to build a healthier, safer world through scientific excellence and client-centric service.

Inotiv, Inc.'s Core Purpose

You're investing in a company whose cultural DNA is built around speed and scientific continuity, not just transactional services. The company's commitment to this is visible in its operational metrics, like the preliminary full-year 2025 revenue projection of between $512.5 million and $513.5 million, which reflects growth driven by this core focus.

Official mission statement

The mission is a direct promise to clients and the broader healthcare ecosystem: deliver exceptional service and products to drive improved decision making, allowing accelerated goal attainment, while providing client-centric scientific continuity in an environment where people are valued and can succeed. That's a mouthful, but it boils down to: Help clients get their drugs to market faster and better.

  • Deliver exceptional service and products.
  • Drive improved decision making for clients.
  • Accelerate goal attainment (drug development).
  • Provide client-centric scientific continuity.

Vision statement

Inotiv's vision is to be a leading contract research organization (CRO) that supports discovery and nonclinical development through the Investigational New Drug (IND) phase and beyond. They want to be the essential partner in the process.

They aim to increase efficiency, improve data quality, and reduce the cost of taking new drugs to market, all while working together to build a healthier and safer world. This isn't just a marketing line; it's a strategic goal. For instance, the company is consolidating its Research Models and Services (RMS) breeding facilities from 20 to 10, which is expected to save $6 to $7 million annually, directly supporting the vision of reducing client costs and improving efficiency.

You can find a deeper dive into these guiding principles here: Mission Statement, Vision, & Core Values of Inotiv, Inc. (NOTV).

Inotiv, Inc. slogan/tagline

While the company doesn't use a single, short tagline everywhere, its client-facing message is clear and action-oriented, reflecting its commitment to quality and service. They are defintely focused on delivering a higher standard of partnership.

  • Expect More From Your Discovery, Development and Research Models Partner.

This is reinforced by their core values, which are the operational rules for every employee:

  • Deliver Excellent Client Experiences.
  • Provide Insightful Problem Solving.
  • Always Do the Right Thing.
  • Be Humbly Confident.
  • Get It Done.

Here's the quick math: The company's Discovery and Safety Assessment (DSA) segment saw awards jump over 60% quarter-over-quarter in Q4 2025, showing that clients are responding to this value proposition of speed and integrated science.

Inotiv, Inc. (NOTV) How It Works

Inotiv, Inc. operates as a crucial link in the pharmaceutical and medical device supply chain, functioning as a contract research organization (CRO) that accelerates drug discovery and preclinical development for its clients. It makes money by providing specialized nonclinical testing services and supplying high-quality research models, which together help researchers make fast, data-driven go/no-go decisions on new therapies.

Inotiv, Inc.'s Product/Service Portfolio

The company's operations are divided into two primary segments: Discovery and Safety Assessment (DSA) and Research Models and Services (RMS). For the full fiscal year 2025, Inotiv anticipates consolidated revenue to be between $512.5 million and $513.5 million, demonstrating the scale of these combined offerings.

Product/Service Target Market Key Features
Discovery & Safety Assessment (DSA) Services Pharmaceutical, Biotech, and Medical Device Developers Nonclinical and analytical testing; includes toxicology, Drug Metabolism and Pharmacokinetics (DMPK), bio-analytical testing, and histopathology. The DSA services business had a backlog of approximately $138.0 million at the end of FY 2025.
Research Models & Services (RMS) Academic, Government, and Commercial Research Institutions Supply of research models (e.g., non-human primates, rodents); includes colony management, custom breeding, and health monitoring services. RMS revenue saw a 34.1% increase in Q3 FY 2025 compared to the prior year.
Ancillary Research Products Research Laboratories and Animal Facilities Teklad™ custom and standard diets, bedding, and environmental enrichment products.

Inotiv, Inc.'s Operational Framework

The operational framework focuses on integrating the two core segments to offer a seamless, end-to-end preclinical solution for clients. This integration is key to creating value, especially as the company works to unify its operations under one brand.

  • Integrated Service Flow: Research models from the RMS segment are supplied directly to the DSA labs, streamlining the drug development process and reducing logistics friction for clients.
  • Site Optimization: The company is executing site optimization plans for its North American facilities to align better with evolving client business models and improve overall efficiency.
  • Client-Centric Contract Awards: The DSA services business is showing strong contract momentum, with a full-year fiscal 2025 book-to-bill ratio anticipated to be approximately 1.05x. That's a defintely healthy sign of demand outpacing service delivery in the near-term.
  • Supply Chain Control: Efforts are underway to optimize North American transportation and distribution systems to ensure a smoother, more reliable experience for the delivery of research models and products.

Inotiv, Inc.'s Strategic Advantages

In a crowded Contract Research Organization (CRO) sector, Inotiv's competitive edge comes from its unique combination of specialized services and its direct control over the supply of critical research models.

  • Single-Source Preclinical Partner: By owning both the research models and the nonclinical testing services, Inotiv eliminates intermediaries, which simplifies logistics, improves data integrity, and speeds up the research timeline for clients.
  • Scientific Specialization: The company offers top-notch bio-analytical capabilities and fit-for-purpose drug testing approaches, including fully GLP (Good Laboratory Practices)-validated methods, which are essential for regulatory submissions.
  • Focus on Early-Stage Development: Inotiv concentrates on the high-value, early-stage discovery and preclinical phases, helping biotech firms mitigate downstream risk by identifying unfavorable attributes early on.
  • NHP Supply Stability: Strategic initiatives like expanding the non-human primate (NHP) client base and securing pre-sales for calendar year 2025 are aimed at reducing revenue volatility and stabilizing the Research Models and Services segment.

If you want to dig deeper into the ownership structure behind these segments, you should check out Exploring Inotiv, Inc. (NOTV) Investor Profile: Who's Buying and Why?

Inotiv, Inc. (NOTV) How It Makes Money

Inotiv, Inc. generates revenue primarily by acting as a critical, outsourced partner in the drug discovery and development pipeline for pharmaceutical, biotech, and medical device companies. They essentially make money from two distinct but highly complementary streams: selling specialized research models and providing nonclinical laboratory testing services that move a drug candidate from the lab bench toward human trials.

Inotiv, Inc.'s Revenue Breakdown

Looking at the nine months ended June 30, 2025 (YTD FY2025), Inotiv, Inc.'s revenue stream is clearly dominated by the supply side of the business, though the services segment is showing strong booking momentum. Here's the breakdown of the $374.9 million in year-to-date revenue:

Revenue Stream % of Total Growth Trend
Research Models & Services (RMS) 63.6% Increasing (6.1% YTD FY2025)
Discovery & Safety Assessment (DSA) 36.4% Stable/Increasing (0.6% YTD FY2025)

Business Economics

The core economics of Inotiv, Inc. center on high-value, specialized assets and a services business model that prioritizes utilization and backlog. The Research Models and Services (RMS) segment, which drove 63.6% of YTD FY2025 revenue, is heavily influenced by the supply and pricing of Non-Human Primates (NHP) and other research models. The significant increase in RMS revenue is mainly due to higher NHP-related product and service revenue, a critical, high-barrier-to-entry market.

The Discovery and Safety Assessment (DSA) segment operates on a services-based model, where pricing stability is key. The company is seeing a much more stable pricing environment across its DSA services, a good sign that market capacity adjustments have firmed up pricing over the past 18 months. This segment's health is best tracked by the book-to-bill ratio, which was a robust 1.07x in Q3 FY2025, meaning they booked $1.07 in new business for every $1.00 of revenue recognized. That's a clear indicator of future revenue growth.

  • DSA Backlog: The services backlog stood at approximately $138.0 million as of September 30, 2025, up from $129.9 million a year prior, which provides a strong, visible revenue pipeline for the coming quarters.
  • Cost Management: Inotiv, Inc. is actively optimizing its cost structure by reducing its RMS breeding facilities from 20 to 10, a move expected to generate $6 million to $7 million in annual net savings by March 2026.
  • Capital Spending: The company anticipates its capital expenditures (CapEx) for the full fiscal year 2025 will be less than 4% of total revenue, suggesting a focus on operational efficiency and debt management over aggressive expansion.

Inotiv, Inc.'s Financial Performance

While the company is a critical part of the drug development ecosystem, its financial performance in FY2025 shows a business in transition, focusing on operational improvements and margin recovery. For the nine months ended June 30, 2025, total revenue climbed to $374.9 million, a 4.0% increase year-over-year. Here's the quick math on the bottom line:

  • Net Loss: The consolidated net loss for YTD FY2025 was $60.1 million, a significant improvement from the $90.0 million loss in the prior year period.
  • Adjusted EBITDA: Adjusted Earnings Before Interest, Taxes, Depreciation, and Amortization (EBITDA)-a key measure of operational cash flow-was $22.1 million for YTD FY2025, or 5.9% of total revenue. This is a positive trend, up from $12.8 million (3.6% of total revenue) in the same period last year.
  • Liquidity and Debt: The company's total debt (net of debt issuance costs) was approximately $396.0 million as of December 31, 2024. The high debt-to-equity ratio of 3.12 and an Altman Z-Score of -0.54 signal financial distress and a need for successful debt restructuring, which management is actively pursuing.
  • Valuation: Despite the operational growth in DSA, the market remains skeptical, reflected in a high Enterprise Value to EBITDA ratio of 21.97 as of November 2025.

You can get a deeper dive into the balance sheet and cash flow dynamics here: Breaking Down Inotiv, Inc. (NOTV) Financial Health: Key Insights for Investors

Inotiv, Inc. (NOTV) Market Position & Future Outlook

Inotiv, Inc. holds a niche but growing position in the highly fragmented non-clinical Contract Research Organization (CRO) market, leveraging its integrated Discovery and Safety Assessment (DSA) services with its Research Models and Services (RMS) segment. The company's future outlook hinges on successful debt restructuring and realizing the operational efficiencies from its strategic site consolidations, aiming for a stronger margin profile despite a challenging funding environment for early-stage biotech clients.

Competitive Landscape

The global preclinical CRO market is valued at approximately $6.80 billion in 2025, and Inotiv, Inc. is a mid-sized player competing against much larger, integrated drug development giants. Our estimate for Inotiv, Inc.'s share is based on its anticipated full-year 2025 revenue of approximately $513.0 million, placing it in the high-growth, specialized segment of the market.

Company Market Share, % Key Advantage
Inotiv, Inc. 7.5% Integrated Research Models & Services (RMS) supply chain and non-clinical expertise
Charles River Laboratories 37% Dominant scale in safety assessment and proprietary, extensive animal model capabilities
Labcorp (Early Development) 46% Integrated diagnostics and drug development platform, massive global scale and reach

The competitive pressure is intense, particularly from the industry leaders that offer full-service, end-to-end solutions. Inotiv, Inc.'s core competitive advantage is its vertical integration of the RMS and DSA segments, offering a single-source solution that streamlines the preclinical process for its clients. You can read more about the foundation of their strategy here: Mission Statement, Vision, & Core Values of Inotiv, Inc. (NOTV).

Opportunities & Challenges

The near-term focus is less on revenue growth and more on margin improvement and balance sheet repair. That's the real story.

Opportunities Risks
Strong demand for Discovery and Safety Assessment (DSA) services, with a positive FY 2025 book-to-bill ratio of roughly 1.05x. Significant debt load and the critical need to refinance or restructure debt to improve financial health.
Realizing annualized cost savings of $6-$7 million from reducing RMS breeding facilities from 20 to 10 by February 2026. Compliance risks and financial commitments stemming from the U.S. Department of Justice's Resolution and Plea Agreements.
Consolidating software platforms from 260 to 150 to drive operational efficiency and better cross-selling between segments. Ongoing operational and reputational impacts from the recent cybersecurity incident in Q4 FY 2025.

Industry Position

Inotiv, Inc. is positioned as a critical, mid-tier preclinical partner, especially for small-to-mid-sized biotechnology firms that prefer an integrated service model. While the company's 7.5% estimated share of the preclinical CRO market is small compared to the market behemoths, its focus on non-clinical and early-phase development allows it to capture specialized demand.

  • Niche Specialization: The company is a leader in the non-human primate (NHP) research model market, a segment with high barriers to entry and supply chain volatility, which provides defintely pricing power when supply stabilizes.
  • Asset Rationalization: The aggressive reduction in RMS site footprint is a clear move to shift from a high-cost, asset-heavy model to a more capital-efficient service provider, aiming to boost the adjusted EBITDA margin.
  • Backlog Visibility: The DSA segment's anticipated backlog of approximately $138.0 million as of September 30, 2025, provides solid revenue visibility for the coming quarters, which is a key indicator of sustained client demand.

The next concrete step for you is to monitor the December 2025 earnings call for the final, audited FY 2025 results and, more importantly, the details of the debt restructuring plan.

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