Gitnux/Report 2026

Biosimilar Industry Statistics

The global biosimilar market is estimated at $46.4 billion in 2026, explore the figures behind growth, companies and trends.
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Samuel NorbergWritten by Samuel Norberg·Fact-checked by Maya Johansson
Published
How this report is researched
01Editorial Scope

Before any source is gathered, an editor locks the question, what qualifies, and how the piece will be judged.

02Source Research

Search agents collect the source set and pull each data point out with its provenance attached.

Read our full methodology →

Search agents attach provenance to every extracted figure.

Next review: within 31 days

01 Industry overview

The biosimilar industry at a glance

The global biosimilar market is estimated at $46.4 billion in 2026, as patent expiries, expanding approvals and lower-cost competition accelerate adoption across North America, Europe and Asia-Pacific.

$46.4B[61]
Global market size, 2026
18.4%[61]
Forecast CAGR, 2026–2033
41[62]
EU biosimilars approved, 2025
$20.2B[44]
U.S. biosimilar savings, 2024
Market size
The global biosimilars market was valued at $39.6 billion in 2025 and is estimated at $46.4 billion in 2026. IQVIA estimated the European biosimilar market at about $18 billion and the U.S. market at about $12 billion at list prices in Q3 2025.[61][13]
Forecast & CAGR
Grand View Research forecasts the global market to reach $151.6 billion by 2033, implying an 18.4% CAGR from 2026 to 2033. A separate 2026 estimate projects $185.2 billion by 2035 at a 16.6% CAGR from 2026 to 2035, reflecting differences in market definitions and methodology.[61][63]
Market share & regions
North America accounted for 42.6% of global biosimilar revenue in 2025 in Grand View Research’s estimate. IQVIA reported approximately $18 billion in European biosimilar sales versus $12 billion in the United States and about $1 billion in China at Q3 2025 list prices; Asia-Pacific is identified as the fastest-growing major region in the forward market forecast.[61][13]
Segmentation
Monoclonal antibodies were the largest drug-class segment, with 44.9% of 2025 revenue; autoimmune disorders led indications with 39.9%; and hospitals represented 52.3% of end-use revenue. The principal market segments are organized by drug class, indication, end user and geography.[61]
Key players & concentration
The market includes Sandoz, Pfizer, Amgen, Celltrion, Biocon, Viatris, Samsung Bioepis, Teva and Dr. Reddy’s Laboratories. One 2026 market estimate places Sandoz above 18% share in 2025 and estimates that its five leading companies held 55% combined share, indicating substantial but not complete concentration.[63][61]
Pricing
U.S. biosimilars generated $20.2 billion in savings in 2024 and $56.2 billion cumulatively since the first U.S. biosimilar entered in 2015. Pricing pressure is significant but uneven: FDA said in October 2025 that biosimilars’ U.S. market share remained below 20%, indicating that lower prices do not automatically translate into rapid substitution.[44][50]
Trends, drivers & challenges
An estimated 118 biologics are expected to lose U.S. patent protection during 2025–2034, representing a potential $232 billion opportunity for biosimilars. Growth is supported by patent expiries and cost pressure, while development economics, formulary access, reimbursement design and limited pipeline coverage remain constraints; an industry assessment says fewer than 15 of more than 100 brand biologics are currently expected to have biosimilar development.[13][50]
Consumer behavior & competition
Competition is broadening at the molecule level: FDA reported 81 biosimilars for 20 reference products by 2025, including 10 for Humira, 9 for Prolia and Xgeva, and 8 for Stelara. Despite this supply, FDA reported U.S. biosimilar market share below 20% in October 2025, showing that prescribing, payer formularies, interchangeability and provider incentives remain important adoption factors.[50]
Regulation
The U.S. biosimilar pathway was created by the 2010 Biologics Price Competition and Innovation Act. In October 2025, FDA proposed reducing unnecessary clinical testing and making it easier to develop biosimilars as interchangeable products; in the EU, the EMA reported that its committee approved 41 biosimilars in 2025, the highest annual number to date.[50][62]
Latest news
The most significant recent regulatory development was FDA’s October 29, 2025 announcement of draft guidance to accelerate biosimilar development and reduce clinical-testing requirements. The agency said it had approved 76 biosimilars at that date, while its 2025 approval report later recorded 81 approved biosimilars for 20 reference products.[50]

02 Ranking

Top 10 Companies in the Biosimilar Industry

The leading companies in the biosimilar industry, ranked on market impact, performance, momentum, innovation and brand popularity.

Updated November 11, 2026 · Next review December 11, 2026

Verdict

Celltrion stands out for global antibody biosimilars and biologics because it delivered revenue growth of 17% and an operating margin of 28.1%, while Samsung Biologics focuses on biosimilars through Samsung Bioepis since its biosimilars were treating patients across 39 countries.

Ranked by Overall score · How we score ↓

Editor's top 3 picks

Where to start, by need.

  1. #1 Overall · Leader in antibody biosimilars

    Celltrion

    KR

    Ranked #1 · 9.1 · Antibody biosimilars

    Why we picked it: It is built around global antibody biosimilars and biologics, with 17% revenue growth and 28.1% operating margin.

    See in ranking ↓Visit celltrion.com ↗

  2. #2 overall

    Samsung Biologics

    KR

    Ranked #2 · 9.1 · Antibody biosimilars

    Why we picked it: It operates biosimilars through Samsung Bioepis, including treatment across 39 countries alongside 30.3% revenue growth.

    See in ranking ↓Visit samsungbiologics.com ↗

  3. #3 overall

    Amgen

    US

    Ranked #3 · 9.1 · Antibody biosimilars

    Why we picked it: It reports $3.0 billion in biosimilars sales in 2025 while maintaining an operating margin of 24.7%.

    See in ranking ↓Visit amgen.com ↗

Pick 1 is the #1 company overall. No other segment places in the top 5, so picks 2 and 3 follow rank.

Full ranking

Sort by
Top 10 companies in the biosimilar industry, 2026 – Gitnux ranking
#CompanyOverall ↓Company snapshot
1

Celltrion

Antibody biosimilars · KR

9.1
2

Samsung Biologics

Antibody biosimilars · KR

9.1
3

Amgen

Antibody biosimilars · US

9.1
4

Sandoz

Antibody biosimilars · CH

8.9
5

Pfizer

Antibody biosimilars · US

8.8
6

Alvotech

Biosimilar development and manufacturing · IS

8.6
7

Shanghai Henlius Biotech

Chinese antibody biosimilars and biologics · CN

8.5
8

Bio-Thera Solutions

Chinese biosimilars and biologics · CN

8.1
9

Fresenius Kabi

Global biosimilars and biopharmaceuticals · DE

8.0
10

Xbrane Biopharma

Specialty and ophthalmic biosimilars · SE

7.5

How we score

  • Impact (30%): scale and weight in the market (revenue, market share, employees, market position).
  • Performance (20%): recent revenue growth and operating margin; an analyst assessment where a company does not publish them.
  • Momentum (20%): growth trajectory and future potential.
  • Innovation (15%): R&D intensity and how technologically advanced the company is.

Popularity (brand search demand, 15%) counts toward Overall but is not published as a column. Overall leaves out what is not known.

Scale Scores are shown on a 7–10 scale with one decimal; bars start at 7.0.

Cadence Recalculated when new figures are published; next review December 11, 2026.

Independence. Rankings are editorially independent. Scores, ranks, picks and the verdict follow the method above; no company can pay to change them.

Cite this ranking

APA

Samuel Norberg. (2026, November 11). Top 10 companies in the biosimilar industry. In Biosimilar Industry Statistics. Gitnux. https://gitnux.org/biosimilar-industry-statistics/#top-companies

report visual · Comparison

Biosimilars' share of the total pharmaceutical market (Europe)

Netherlands leads with 22%.

Netherlands22%
Sweden20%
Denmark14%
France12%
Spain10%
Italy8%
source-verifiediqvia.com

04 Statistics

Technology & Innovation

In technology & innovation, robotics and automation adoption reached 63% in 2023, while 70% of global biopharma respondents adopted an R&D data platform in 2023.

Digital Transformation in the pharmaceuticals and biotech sector (sector benchmark)

  • 13% of clinical-research organizations surveyed reported a comprehensive AI-driven digital programme in 2024.[1]
  • 58.1% of global pharmaceutical-industry survey respondents were in the pilots or systematic-ongoing-actions stages of Pharma 4.0 adoption in 2023.[2]
  • 15.1% of global pharmaceutical-industry survey respondents reported that Pharma 4.0 digital transformation had not started in 2023.[2]
  • 45% of pharmaceutical companies surveyed were pursuing digitalization as an innovation or technology in 2024.[3]
  • 35% of clinical-research organizations surveyed were piloting digital technologies in 2024, up from 29% in 2019.[1]

Technology Adoption in the pharmaceuticals and biotech sector (sector benchmark)

  • 63% of global biopharma respondents had adopted robotics and automation in 2023.[4]
  • 70% of global biopharma respondents had adopted an R&D data platform in 2023.[4]
  • 37% of small biopharma respondents reported that more than 60% of their R&D laboratory instruments had automated data capture in 2024.[5]
  • 55% of biopharma AI adopters reported using AI in process development in 2024.[6]
  • 59% of global biopharma respondents had adopted artificial intelligence or machine learning in 2023.[4]

Cloud Computing in the pharmaceuticals and biotech sector (sector benchmark)

  • 18% of global biopharma respondents had adopted cloud-based scientific software or SaaS in 2023.[4]
  • 77% of life-sciences commercial IT leaders reported investing primarily in cloud infrastructure in 2024.[7]
  • 49% of biopharma survey respondents reported using cloud computing to facilitate day-to-day work in 2021.[8]
  • 23% of small biopharma respondents had adopted cloud-based scientific software or SaaS in 2024.[6]
  • 17% of large biopharma respondents had adopted cloud-based scientific software or SaaS in 2024.[6]

Big Data in the pharmaceuticals and biotech sector (sector benchmark)

  • 33% of biopharma survey respondents reported using data lakes in day-to-day operations in 2021.[8]
  • 49% of clinical-research survey respondents reported using AI and big-data analytics in drug development in 2024.[1]
  • 43% of small and midsize pharmaceutical companies surveyed were pursuing big data and analytics in 2024.[3]
  • 48% of pharmaceutical companies surveyed were pursuing big data and analytics in 2024.[3]
  • 55% of large pharmaceutical companies surveyed were pursuing big data and analytics in 2024.[3]
  • 68% of pharmaceutical companies surveyed planned to use advanced analytics in 2024.[9]

IoT in the pharmaceuticals and biotech sector (sector benchmark)

  • 37% of biopharma organizations globally reported using IoT in a project or with a third party in Deloitte’s 2021 survey.[8]
  • 25% of biopharma organizations globally reported using IoT daily in Deloitte’s 2021 digital innovation survey.[8]
  • 53% of global biopharma respondents reported that at least three of five laboratory instruments were connected to software in 2023.[4]
  • 21.4% of IoT-using SMEs in the European healthcare industrial ecosystem applied IoT to predictive maintenance of production assets in 2023.[10]
  • 20.4% of SMEs in the European healthcare industrial ecosystem had adopted Internet of Things technologies in 2023, according to an industry survey.[10]
  • 22.3% of IoT-using SMEs in the European healthcare industrial ecosystem applied IoT to energy-saving devices in 2023.[10]

Innovation in the biosimilar industry

  • 40 biosimilar scientific opinions were issued by the EMA Committee for Medicinal Products for Human Use; 2025, European Union.[11]
  • 151 cumulative biosimilars had been authorised in Europe; 2025, European Union.[11]
  • EUR 13 billion in annual healthcare-system savings was projected from biosimilars in 2024, rising to EUR 16–22 billion annually by 2030; Europe.[11]

05 Statistics

Data & Analytics

In data & analytics, treated-milligrams supply shows broad biosimilar penetration, with biosimilars supplying 83.0% of treated milligrams in Europe in 2025.

Business intelligence in the biosimilar industry

  • The U.S. biosimilar market increased from €6.07 billion in 2020 to an estimated €10.1 billion in 2024.[12]
  • EMA had issued 103 biosimilar approvals during 2006–2025, compared with 69 FDA approvals and 55 NMPA approvals over the same period.[13]
  • The European biosimilar market was worth approximately $18 billion at list prices in Q3 2025, compared with about $12 billion in the United States and $1 billion in China.[13]
  • The Asia-Pacific biosimilar market increased from €1.54 billion in 2020 to approximately €4.53 billion in 2024.[12]

Data analytics in the biosimilar industry

  • 83.0% of treated milligrams in Europe were supplied by biosimilars in 2025 across infliximab, adalimumab, bevacizumab, rituximab and trastuzumab.[14]
  • Biosimilar share of U.S. treated milligrams exceeded 64% for every molecule studied in 2025, ranging from 64.2% for adalimumab to 94.0% for bevacizumab.[14]
  • 40.7% was the average biosimilar market share across 27 European countries in Q1–Q2 2024, compared with 3.6% in 2014.[15]
  • 67.9% of treated milligrams in the United States were supplied by biosimilars in 2025 across five major reference biologics.[14]

Data Quality in the pharmaceuticals and biotech sector (sector benchmark)

  • Across 500 pharmaceutical and biotechnology executives globally, 44% said their organization was prepared on data quality and completeness in 2025.[16]
  • Across 125 senior U.S. life-sciences leaders, 81% said accuracy and confidence in data were critical components of AI success in biopharma in 2026.[17]
  • Across 116 commercial biopharma leaders in the United States, Europe and Asia-Pacific, 81% identified data quality as their top data issue for the next 12 months in 2025.[17]
  • Across 116 commercial biopharma leaders in the United States, Europe and Asia-Pacific, 96% said their data was not well-structured or AI-ready for scaling in 2025.[17]
  • Across 116 commercial biopharma leaders in the United States, Europe and Asia-Pacific, 73% reported significant data quality issues in 2025.[17]

Data Governance in the pharmaceuticals and biotech sector (sector benchmark)

  • Across 200 global life-sciences R&D respondents, 49% called for more data-governance frameworks to make data FAIR at scale in 2024.[18]
  • Across 11 pharmaceutical regulatory organizations, 9% reported a comprehensive approach to onboarding standards such as IDMP and XEVMPD, with regular source qualification, connected systems and data cleaning in 2023.[19]
  • Across 200 global life-sciences R&D respondents, 51% identified maintenance and management of data standards and ontologies as a key FAIR-data need in 2024.[18]
  • Across 500 pharmaceutical and biotechnology executives globally, 54% said their organization was prepared on data governance in 2025.[16]
  • Across 200 global life-sciences R&D respondents, 46% called for templates for standardization and metadata to make data FAIR at scale in 2024.[18]

KPIs in the biosimilar industry

  • Biologics represented 37% of European pharmaceutical expenditure in 2024, while biosimilars represented 4%.[11]
  • The European biosimilar market was 55% larger than the U.S. market at list prices in Q3 2025.[13]
  • The number of EMA CHMP scientific opinions on biosimilars rose from 8 in 2023 to 25 in 2024 and 40 in 2025.[11]
  • Biosimilars represented 4% of the €228 billion European pharmaceutical market in 2024, according to IQVIA MIDAS data.[11]

06 Statistics

Strategy & Growth

In strategy & growth, U.S. uptake is tied to patent-driven opportunity, with an estimated 118 biologics expected to lose U.S. patent protection during 2025–2034.

Growth in the biosimilar industry

  • $189 billion in additional potential U.S. healthcare savings was estimated if biologics expiring during 2025–2034 without a current biosimilar pipeline gained competition.[13]
  • 3.3 billion days of patient therapy had been delivered by U.S. biosimilars since their first market entry in 2015, according to the 2025 savings report.[20]
  • $20.2 billion in U.S. savings were generated by biosimilars in 2024.[20]

Mergers and acquisitions in the biosimilar industry

  • $3 billion was the total consideration Viatris received for contributing its global biosimilars portfolio to Biocon Biologics in November 2022.[21]
  • $373.5 million was the gain Viatris recorded in 2024 from remeasuring its convertible preferred shares in Biocon Biologics to fair value.[21]
  • 12.9% was Viatris’ approximate fully diluted ownership stake in Biocon Biologics at the closing of the 2022 transaction.[21]

Strategic partnerships in the biosimilar industry

  • Up to 5 biosimilar assets were covered by Sandoz and Samsung Bioepis’ March 2026 license, development and commercialization partnership.[22]
  • 32 assets could comprise Sandoz’s biosimilar pipeline after the 2026 Samsung Bioepis partnership, according to Sandoz.[22]

07 Statistics

People & Workforce

In people & workforce, adoption of flexible work is widespread, with 65.9% of U.S. life sciences companies reporting remote-work options for at least some employees in 2023.

Remote Work in the pharmaceuticals and biotech sector (sector benchmark)

  • Among privately held life-sciences companies surveyed, 21.7% had some portion of their workforce fully remote in 2025.[23]
  • Across U.S. life sciences companies, 65.9% reported implementing, expanding, or considering remote-work options for at least some employees in 2023.[24]
  • Across U.S. chemical and pharmaceutical manufacturers, 5.7% of positions were fully remote in the 2024 hiring outlook survey.[25]
  • Among life-sciences companies with remote-work options, 50.0% cited competition with technology and other industries as a reason for their policy in 2023.[24]

Hybrid Work in the pharmaceuticals and biotech sector (sector benchmark)

  • Among surveyed life-sciences companies in the MassBio Human Resources Roundtable, 97% planned to implement hybrid work models for the long term in 2022.[26]
  • Among surveyed life-sciences employers in the BioHealth Capital Region, 60% expected at least a hybrid workforce after the pandemic in 2021.[27]
  • Across U.S. chemical and pharmaceutical manufacturers, 44.5% of positions were fully hybrid in the 2024 hiring outlook survey.[25]
  • Among life-sciences CEOs, 83% expected corporate employees whose roles were traditionally office-based to work in a hybrid environment three years after the 2024 survey.[28]

Employee Engagement in the pharmaceuticals and biotech sector (sector benchmark)

  • Across the Culture Amp pharmaceuticals benchmark, 91% of employees agreed they understood how their work contributed to company goals in July 2026.[29]
  • Across the Culture Amp pharmaceuticals benchmark, 17% of employees disagreed that they had seen positive changes based on recent employee survey results in July 2026.[29]
  • At Amneal Pharmaceuticals, global employee engagement reached 88% in the company’s 2024 reporting year.[30]
  • Across the Culture Amp pharmaceuticals benchmark, 18% of employees were thinking of or actively seeking another job in July 2026.[29]

Change Management in the pharmaceuticals and biotech sector (sector benchmark)

  • Among 125 pharmaceutical and biotechnology executives surveyed, 68% said their organizations were actively increasing investments in change management in 2023.[31]
  • Across pharmaceutical-company respondents, organizations spent almost 14 months planning and initiating clinical-trial innovations before later evaluation, adoption, and implementation stages in 2022.[32]
  • Among pharmaceutical and biotechnology executives surveyed, 26% expected to conduct a significant acquisition within the following 12 months in 2023.[31]
  • Across 612 pharmaceutical-company respondents, clinical-trial innovations took an average of 69 months from planning to portfolio-wide implementation, excluding decentralized-trial adoption during COVID-19.[32]
  • Among pharmaceutical and biotechnology executives surveyed, 69% felt their organizations were well equipped to handle growing pressures in 2023.[31]

08 Statistics

Customer & Sales

In customer & sales, patient decision signals still hinge on clinical communication, with 71% of U.S. patients confident and accepting a biosimilar when their doctor explained the option in 2021.

Customer experience in the biosimilar industry

  • 78% of US patients were very likely to start a biosimilar rather than a brand biologic if their doctor recommended it; 2021, United States.[33]
  • 77% of US patients said they would always accept their doctor’s medication recommendation; 2021, United States.[33]
  • 71% of US patients said they would be fully confident and accept a biosimilar if their doctor explained the option; 2021, United States.[33]
  • 84% of US patients prescribed a biosimilar said they discussed differences between the biosimilar and the brand biologic with their doctor; 2021, United States.[33]
  • 77% of US patients believed biosimilars were equal or better than branded biologics in efficacy; 2021, United States.[33]

Customer retention in the biosimilar industry

  • 19% of US patients initiating adalimumab-adaz switched therapies in a national analysis; 2026, United States.[15]
  • 51.7 switches per 1,000 potentially eligible Humira patients were recorded in April 2024, versus 4.65 per 1,000 in December 2023; United States.[34]
  • 4.9% of 42,612 eligible US Humira patients had switched from the originator to a biosimilar by April 2024; 2024, United States.[34]
  • 76.7% of Humira-to-biosimilar switches during 2024 went to Hyrimoz, the product covered by all CVS formularies; 2024, United States.[34]

Customer acquisition in the biosimilar industry

  • 40% of US patients prescribed biosimilars received them as a new prescription rather than as a replacement for a brand biologic; 2021, United States.[33]
  • 78% of US patients were very likely to initiate a biosimilar instead of a brand biologic when recommended by their doctor; 2021, United States.[33]

Customer loyalty in the biosimilar industry

  • 43% of US current biosimilar users said they would switch to another biosimilar, while 26% would not and 32% were unsure; 2022 survey, United States.[35]
  • 58% of US patients prescribed a biosimilar received it to replace a brand biologic they had previously taken; 2021, United States.[33]

09 Statistics

Marketing & Brand

In marketing & brand, information channels remain practical and clinician-facing, with 48% of physicians learning about newly available biosimilars through journals in a 2023 survey.

Marketing in the biosimilar industry

  • 48% of physicians learned about newly available biosimilars through journals in a 2023 survey of more than 120 U.S. physicians.[36]
  • 56% of physicians learned about newly available biosimilars from colleagues in a 2023 survey of more than 120 U.S. physicians.[36]
  • 42% of physicians learned about newly available biosimilars from sales representatives in a 2023 survey of more than 120 U.S. physicians.[36]

Digital marketing in the biosimilar industry

  • 40% of physicians learned about newly available biosimilars through independent research in a 2023 survey of more than 120 U.S. physicians.[36]
  • 48% of surveyed physicians were very comfortable prescribing biosimilars in a 2023 U.S. physician survey.[37]
  • 31% of surveyed physicians believed biosimilar economics were favorable enough to switch in a 2023 U.S. physician survey.[37]
  • 59% of surveyed healthcare professionals agreed that information is more valuable when it aligns with the patient they are treating, according to a 2023 biosimilar survey.[37]

Branding in the biosimilar industry

  • 50% of surveyed physicians said data, education and resources on biosimilar safety and immunogenicity were a must-have for adoption in the United States.[38]
  • 46% of surveyed physicians felt confident in their ability to use biosimilars in the United States.[38]
  • 70% of surveyed physicians said manufacturer trust and reliability data, education and resources were a must-have for biosimilar adoption in the United States.[38]
  • 68% of surveyed physicians said provider education on biosimilar efficacy and safety was a must-have for adoption in the United States.[38]

Influencer Marketing in the pharmaceuticals and biotech sector (sector benchmark)

  • 29% of healthcare and pharmaceutical marketers reported dedicated but flat budgets for creator or influencer marketing in 2026, globally.[39]
  • 50% of healthcare and pharmaceutical marketers reported dedicated and growing budgets for creator or influencer marketing in 2026, globally.[39]
  • 10% of healthcare and pharmaceutical marketers said they did not invest in creator or influencer marketing in 2026, globally.[39]
  • 50% of physicians in Europe, APAC and North America said healthcare influencer or KOL content had changed their prescribing choices in 2024.[40]
  • 44% of physicians in Europe, APAC and North America said healthcare influencer or KOL content had changed their perception of a medication in 2024.[40]

10 Statistics

Operations & Execution

In operations & execution, vertical integration shifts contracting execution, with 83% of vertically integrated payers reporting integration had been extremely impactful on rebate and contract execution in 2026.

Process optimization in the biosimilar industry

  • $5.1 million in estimated development cost savings could result from allowing a global comparator for biosimilar development, according to a 2025 U.S. policy analysis.[41]
  • $13.5 million in estimated lifetime net revenue could result from allowing a global comparator for biosimilar development, according to a 2025 U.S. policy analysis.[41]
  • $84 million in estimated lifetime net revenue could result from eliminating the comparative efficacy study requirement, according to a 2025 U.S. biosimilar market analysis.[41]
  • $24 million in estimated development cost savings could result from eliminating the comparative efficacy study requirement for biosimilars, according to a 2025 U.S. policy analysis.[41]

Operational efficiency in the biosimilar industry

  • 83% of vertically integrated payers said integration had been extremely impactful on rebate and contract execution in 2026.[42]
  • 81% of surveyed payers reported that their organizations had completed vertical integration efforts in 2026, affecting biosimilar formulary and contracting operations.[42]
  • 70% of surveyed payers said they were highly likely to remove a reference product from preferred formulary status once a biosimilar entered the market in 2026.[42]
  • 64% of surveyed payers included private-label biosimilars from pharmacy benefit managers on formulary in 2026.[42]

Outsourcing / Offshoring in the pharmaceuticals and biotech sector (sector benchmark)

  • 41% of surveyed pharmaceutical and biotech R&D leaders increased their use of functional-service-provider outsourcing versus two years earlier in 2023.[3]
  • 54% of global biotech and pharma companies outsourced regulatory activities in 2024, according to an IQVIA industry report.[13]
  • 74% of surveyed pharmaceutical and biotech R&D leaders ranked patient recruitment among the top five drug-development activities likely to be outsourced in 2023.[3]
  • 12% of total API volume used in the United States was produced domestically in 2024, with most supply coming from India and the European Union.[43]
  • 67% of global biotech and pharma companies outsourced pharmacovigilance operations in 2024, according to an IQVIA industry report.[13]

11 Statistics

Finance & Pricing

In finance & pricing, savings are clear but uneven substitution persists, with U.S. biosimilar market share remaining below 20% in October 2025 per FDA.

Pricing strategy in the biosimilar industry

  • 37% of physicians identified pricing versus the reference product as the most important biosimilar contracting, purchasing or procurement factor in a U.S. physician survey.[38]
  • 50% of surveyed physicians wanted a 20%–30% total cost reduction for a biosimilar to facilitate adoption in the United States.[38]
  • Biosimilars launched with discounts of up to 92% off Humira’s wholesale acquisition cost in the United States in 2023.[20]
  • 70% of surveyed payers rated rebate or net-price guarantees and formulary exclusivity as leading drivers of biosimilar adoption in 2026.[42]

Cost reduction in the biosimilar industry

  • 13%–42% was the observed range of U.S. price reductions over 36 months following biosimilar market entry, based on IQVIA invoice-price data analyzed in 2025.[41]
  • 31% was the average U.S. price reduction over 36 months following biosimilar market entry, based on IQVIA invoice-price data analyzed in 2025.[41]
  • 40% was the approximate average reduction in biosimilar average sales price versus the brand biologic within three years of launch in the United States, reported in 2025.[44]
  • 23% was the average reduction in brand-biologic average sales price three years after biosimilar market entry in the United States, reported in 2025.[44]

Profitability in the biosimilar industry

  • $2 billion was the estimated increase in lifetime net revenue if all approved biosimilars were designated interchangeable, according to a 2025 U.S. policy analysis.[41]
  • $150 million–$220 million was the estimated margin earned by wholesalers on competitive biologics in the United States, compared with $840 million–$1.09 billion on noncompetitive biologics, in the analyzed period.[41]
  • $9.5 billion was the estimated lifetime net revenue for an average first biosimilar entrant in a large market, according to a 2025 U.S. market-entry analysis.[41]
  • -$33.5 million was the estimated lifetime net revenue for an average biosimilar entrant in a small market, according to a 2025 U.S. market-entry analysis.[41]

Financial planning in the biosimilar industry

  • $28 billion was the estimated potential savings from biosimilar competition for eight biologic medicines in the United States through 2024, including savings that could have occurred for Humira and Enbrel.[45]
  • $13 billion–$66 billion was the estimated range for U.S. direct biologic-drug spending reductions from biosimilars between 2014 and 2024 in an early economic forecast.[15]
  • $44 billion was the estimated reduction in U.S. direct biologic-drug spending from biosimilars between 2014 and 2024 in an early economic forecast.[15]
  • $100 million–$300 million was the estimated research and direct-outlay cost required to develop a competitive biosimilar, according to a 2024 industry analysis.[45]

12 Statistics

Product & Service

In product & service, development economics remain dominated by clinical work, with 57% of total biosimilar development cost represented by clinical development in an analytical framework.

Product development in the biosimilar industry

  • 57% of total biosimilar development cost is represented by clinical development in an analytical investment framework covering three monoclonal-antibody programs.[15]
  • 5–7 years is the average duration of biosimilar development globally, according to an IQVIA analysis published in 2024.[11]
  • 60%–70% of total biosimilar development cost in India is attributed to clinical studies, while U.S. or EU authorization can cost approximately $25 million per product.[46]

Product lifecycle in the biosimilar industry

  • The European biosimilar sector contributed €25.6 billion to European GDP in 2024, approximately 6% of the pharmaceutical industry's total contribution.[11]
  • 71% of biologics losing exclusivity in Europe between 2024 and 2030 had no biosimilar pipeline identified as of November 2024.[11]
  • The global forecast-sales value of the biosimilar development gap associated with biologics losing exclusivity by 2032 is approximately €122 billion.[11]
  • 79% of approximately 100 biologics expected to lose exclusivity by 2032 had no biosimilars in development, according to a 2026 European Commission analysis.[11]

After-sales in the biosimilar industry

  • Approximately 40% of biologic-naive ulcerative-colitis patients remained on SB5 at 12 months in the PERFUSE study.[15]
  • 88% of 99 U.S. members who transitioned from Humira to an adalimumab biosimilar maintained biosimilar therapy in a 2026 real-world analysis.[47]
  • Approximately 60% of patients remained on adalimumab biosimilar SB5 at 12 months across most populations in the PERFUSE real-world study.[15]
  • Only 26% of surveyed patients reported that their health plan always provides the information needed about biosimilars, while 21% reported high support from their clinical care team.[14]

Value proposition in the biosimilar industry

  • €75 billion in cumulative savings from biosimilar competition had been generated in Europe since 2006, including €13 billion in 2024.[12]
  • $12.4 billion in U.S. savings was generated by biosimilars in 2023 alone, according to the Association for Accessible Medicines.[48]
  • Biosimilars generated nearly $36 billion in U.S. healthcare-system and patient savings from 2015 through 2023.[48]
  • Approximately 1.10 million additional patient-years could have been funded by biosimilar price reductions through 2025 on a constant 2016 budget in the United States and Europe.[14]

14 Statistics

Globalization & Expansion

In globalization & expansion, scale in clinical use is reported via Sandoz biosimilars, with 1.3 billion patient treatment days of cumulative clinical-use experience by 2025.

Supplier management in the biosimilar industry

  • 1.3 billion patient treatment days represented Sandoz biosimilars’ cumulative clinical-use experience by 2025.[22]
  • $2 billion in cash and approximately $1 billion in convertible preferred shares comprised Viatris’ consideration for contributing its biosimilar portfolio to Biocon Biologics in 2022.[21]

Stakeholder management in the biosimilar industry

  • 24 European countries encouraged or mandated prescriber switching from originator biologics to biosimilars or between biosimilars in a 2024 policy analysis.[15]
  • 11 European countries permitted biosimilar substitution at pharmacy level in the policy analysis covering 2024.[15]
  • 15 European countries applied prescribing quotas for biosimilars in the policy analysis covering 2024.[15]

Key questions about the biosimilar industry

What is the 2026 global biosimilar market size?
The global biosimilar market is estimated at $46.4 billion in 2026, as patent expiries, expanding approvals, and lower-cost competition accelerate adoption.
How fast is the market expected to grow after 2026?
Forecast CAGR is 18.4% for 2026–2033, with a projected market reaching $151.6 billion by 2033.
Which companies lead the biosimilar industry?
Celltrion stands out for global antibody biosimilars and biologics because it delivered revenue growth of 17% and an operating margin of 28.1%, while Samsung Biologics focuses on biosimilars through Samsung Bioepis since its biosimilars were treating patients across 39 countries.
What technology shifts are shaping biosimilar operations and data use?
Global biopharma adoption includes robotics and automation (63% in 2023) and R&D data platform adoption (70% in 2023). In commercial data, 96% said their data was not well-structured or AI-ready for scaling in 2025.
What do U.S. biosimilar savings indicate about pricing and adoption?
U.S. biosimilars generated $20.2 billion in savings in 2024 and $56.2 billion cumulatively since the first U.S. biosimilar entered in 2015. Even with pricing pressure, FDA said U.S. market share remained below 20% in October 2025.
Reference

Cite This Report

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APA
Samuel Norberg. (2026, November 11). Biosimilar Industry Statistics. Gitnux. https://gitnux.org/biosimilar-industry-statistics
MLA
Samuel Norberg. "Biosimilar Industry Statistics." Gitnux, 11 Nov 2026, https://gitnux.org/biosimilar-industry-statistics.
Chicago
Samuel Norberg. 2026. "Biosimilar Industry Statistics." Gitnux. https://gitnux.org/biosimilar-industry-statistics.

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