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Chime Biologics

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uuid0000ycv

Namestring
Chime Biologics
Legal namestring
Chime Biologics (Wuhan) Co., Ltd.
Company typeenum
Private
Founded yearint
2013
Descriptiontext

Chime Biologics is a privately held biologics contract development and manufacturing organization (CDMO) founded in 2013 and headquartered in Wuhan, China, with additional operations in Shanghai (China Innovation Hub), Basel (European Innovation Hub opened June 2025), and sales offices in San Diego, Boston, and Paris. The company operates the world's first KUBio modular biopharmaceutical factory built with GE/Cytiva technology, using single-use bioreactors at 50L, 200L, 500L, and 2000L cGMP scales to manufacture monoclonal antibodies, bispecific antibodies, fusion proteins, conjugated proteins, enzymes, and vaccines. Its facilities are designed to meet NMPA, EMA, US FDA, and EU PIC/S GMP standards, and the company reports more than 70 successful 2000L GMP production batches and clinical material supply to clients across 30+ countries.

The company's service portfolio spans the full biologics development lifecycle: cell line development, process development, protein science, technology transfer, drug substance manufacturing, drug product manufacturing (including liquid fill, lyophilized fill and pre-filled syringe fill in isolators), quality systems, regulatory support, project management, and data integrity. In November 2025 it launched the Chime AI Platform in partnership with Opq Therapeutics, adding AI-enabled target screening, antibody design and optimization, AI-enhanced cell line development, and AI-integrated rapid CMC as adjacent offerings. The business operates on professional-services contracts with biotech and biopharmaceutical clients, priced project-by-project, and pursues co-development and strategic partnerships (e.g., Polpharma Biologics, SunRock Biopharma, Domain Therapeutics, Daewoong Pharmaceutical, Libang Pharmaceuticals, TNAX Biopharma) as a parallel go-to-market channel.

Chime generates revenue through negotiated CDMO contracts and strategic collaborations with global biotech and biopharmaceutical clients. Pricing is quote-based and varies with scope, scale and development stage, typical of the contract manufacturing industry. The company is scaling aggressively: a US$190 million Series A+ in May 2024 (led by VMS Group with Fidelity International and Panacea Venture) and a December 2025 Optics Valley Financial Holdings round are funding capacity expansion toward 140,000+ liters over five years, while the Chime Innovation Alliance and Basel hub extend its commercial reach across China, Europe, and APAC.

Short descriptiontext

Chime Biologics is a privately held Chinese CDMO providing end-to-end biologics development and manufacturing — from cell line development through commercial drug substance and drug product supply — serving global biotech and pharmaceutical clients across 30+ countries via its Wuhan KUBio modular facility and Basel European Innovation Hub.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersWuhan, China
HQ citystring
Wuhan
HQ countrystring
China
HQ regionstring
Asia
Markets served

Serves global market

Offices6 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
biologics contract manufacturing, CDMO services, drug substance manufacturing, cell line development, biopharmaceutical development
Industry4 codes
1Biologics (mAbs/Recombinant Proteins) CDMO
CodeHLAGABACPrimaryYes
2Biologic API/Drug Substance Manufacturing Services
CodeHLAAAKAAPrimaryNo
3Process Development & Tech Transfer Services (upstream/downstream)
CodeHLAAAKAFPrimaryNo
4Sterile Fill-Finish & Aseptic Manufacturing CDMO
CodeHLAGABAHPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Pharmaceutical Preparation Manufacturing325412
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Biopharmaceutical Contract Manufacturing (CDMO)
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1CDMO Contract Manufacturing Services
TypeProfessional Services
Description

Full-suite contract development and manufacturing organization (CDMO) services including cell line development, process development, protein science, technology transfer, drug substance manufacturing, drug product manufacturing, quality control/assurance, regulatory support, and project management. Revenue generated through service contracts and manufacturing agreements with biotech and pharmaceutical clients across the development lifecycle from preclinical through commercial stages.

chimebiologics.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Personnel, Infrastructure, Technology or R&D, Operations, Supply Chain, Marketing or Sales
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

Chime Biologics is a global Contract Development and Manufacturing Organization (CDMO) that provides end-to-end biologics manufacturing services for biotech and pharmaceutical companies. The company offers services spanning cell line development, process development, drug substance manufacturing (50L–2000L), drug product manufacturing, technology transfer, quality control, and regulatory support from pre-clinical through commercial stages. Its operations leverage the world's first GE KuBio modular biopharmaceutical manufacturing facility using single-use bioprocessing technology, complemented by the newly launched Chime AI Platform for AI-driven biologics discovery and development.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • Successfully completed over 70 batches of 2000L GMP production
+2 more records
Product overview1 text field

Chime Biologics is a leading global CDMO (Contract Development and Manufacturing Organization) providing end-to-end biologics manufacturing services from pre-clinical support through clinical and commercial manufacturing. The portfolio consists of core service modules including Cell Line Development, Process Development, Protein Science Group, Technology Transfer, Drug Substance Manufacturing (M-DS), Drug Product Manufacturing (M-DP), Quality System, Regulatory Support, Project Management, and Data Integrity. These services are powered by key technology platforms: the KUBio modular biopharmaceutical factory (world's first modular facility using single-use bioreactors from GE/Cytiva), and the Chime AI Platform for AI-driven biologics development. Manufacturing capabilities span scales from 50L to 2000L bioreactors for diverse molecule types including monoclonal antibodies, bispecific antibodies, fusion proteins, conjugated proteins, enzymes, and vaccines.

Product and service1 record
1End-to-End CDMO Services
Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership10 partners
1Beijing Libang Pharmaceutical (Libang Pharmaceuticals)
Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2025-12-10
Description

Strategic collaboration to develop a biosimilar to Amgen's Blincyto (blinatumomab) for global markets. Chime Biologics will leverage its GMP manufacturing platform and regulatory expertise to support the biosimilar development program.

insights.citeline.com
Strategic tierRegionalTypeStrategic or Co-development PartnerAnnounced on2025-12-09
Description

Strategic collaboration marking Chime Biologics' first partnership in Japan. TNAX Biopharma is a Japanese biotech company.

3Opq Therapeutics (奥泊生科)
Strategic tierStrategicTypeTechnology or IntegrationAnnounced on2025-11-02
Description

Strategic collaboration on AI-driven biologics discovery. Opq provides advanced AI technology for target screening, antibody design, and optimization while Chime provides CMC capabilities. Co-founders include Nobel Laureate Michael Levitt.

chimebiologics.com
Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2025-10-21
Description

Strategic collaboration to develop SRB5, a novel anti-CCR9 monoclonal antibody targeting inflammatory bowel disease (IBD) with potential expansion into other immune-mediated inflammatory indications. SunRock Biopharma is a Spanish biotech company focused on next-generation therapeutic antibodies.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-06-06
Description

Host facility for Chime Biologics' European Innovation Hub in Basel. Superlab Suisse provides laboratory space and infrastructure enabling Chime's operations in the heart of Europe's biotech ecosystem.

Strategic tierSupportingTypeStrategic or Co-development PartnerAnnounced on2025-06-06
Description

Basel Area Business and Innovation is the official economic development agency for the Basel area. They support and promote the biotech ecosystem and welcomed Chime Biologics' establishment of European Innovation Hub in Basel.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-06-06
Description

Alliance of leading Chinese biotech service providers providing one-stop solutions for customers from drug discovery through preclinical, clinical, and commercial stages. Partner companies include Sepax Bioscience, AnLing, Alioth Biotech, NanoMicro, Duoning Biotech, Lisure, and others.

8Japan-China Bio-Innovation Ecosystem Forum Partners
Strategic tierSupportingTypeStrategic or Co-development PartnerAnnounced on2025-05-22
Description

Co-organized with Duoning Biotech and Lisure to promote innovation, collaboration, and investment between Japan and China in the biopharmaceutical industry.

chimebiologics.com
Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2025-04-16
Description

Strategic partnership with Poland-based Polpharma Biologics to support end-to-end development and manufacture of a biosimilar product for the global market. Chime provides integrated support from IND stage through commercial supply. Polpharma has two biosimilars approved by FDA and EMA.

Strategic tierMajorTypeStrategic or Co-development PartnerAnnounced on2024-03-12
Description

Manufacturing agreement for DT-7012, a novel anti-CCR8 antibody for cancer immunotherapy. Chime provides cell line development, process development, scale-up, and Phase I GMP clinical manufacturing. DT-7012 is a potential best-in-class Treg-depleting antibody.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers8 records
TypeBroad incumbent
Description

Swiss-based global CDMO with extensive biologics manufacturing capabilities across mammalian and microbial platforms. Serves as the dominant Western incumbent in biologics CDMO, competing with Chime for large-pharma and biotech contracts across multiple regulatory jurisdictions.

TypeDirect peer
Description

Korean-based global biologics CDMO with large-scale cGMP manufacturing capacity (expanding toward ~1M liters) and full lifecycle services from clinical to commercial supply. Direct competitor for global biotech CDMO contracts with overlapping mAb and bispecific capabilities.

TypeDirect peer
Description

China-headquartered, Hong Kong-listed global biologics CDMO offering end-to-end services from cell line development through commercial manufacturing. The most direct competitor to Chime Biologics in terms of geographic origin, service portfolio, and target customer base, with materially larger scale (~600,000L capacity).

TypeDirect peer
Description

Global biologics CDMO with manufacturing sites in the US, Europe, and Japan, offering mammalian and microbial-based biologics development and manufacturing services. Comparable mid-large tier peer competing for similar global biotech CDMO engagements.

TypeDirect peer
Description

Taiwan-headquartered CDMO with rapidly expanding biologics manufacturing capabilities alongside its established small-molecule franchise. Emerging direct competitor in Asia-Pacific biologics CDMO space with similar growth-oriented capacity expansion trajectory.

TypeBroad incumbent
Description

Large US-headquartered CDMO with biologics fill-finish, cell line, and biomanufacturing capabilities as part of a broader services portfolio. Overlaps with Chime on biologics drug substance and drug product manufacturing while also serving injectables, oral, and inhalation delivery.

TypeDirect peer
Description

US-headquartered biologics CDMO (acquired by JSR Life Sciences) offering process development, analytical services, and cGMP manufacturing. Comparable mid-tier peer with similar focus on mammalian cell-based biologics and competitive pressure in the same customer segment.

TypeDirect peer
Description

German-headquartered biologics CDMO division of Boehringer Ingelheim offering contract manufacturing from cell line through commercial supply. Direct peer with comparable service portfolio and similar positioning in mammalian-cell biologics manufacturing for global biotech clients.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI capability4 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles4 records

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Name, Designation, Designation category, Overview, Profile commentary, Source

No data
Compliance6 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds4 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors5 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment1 record

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Chime Biologics

Biopharmaceutical Contract Manufacturing (CDMO)chimebiologics.com

Chime Biologics is a privately held Chinese CDMO providing end-to-end biologics development and manufacturing — from cell line development through commercial drug substance and drug product supply — serving global biotech and pharmaceutical clients across 30+ countries via its Wuhan KUBio modular facility and Basel European Innovation Hub.

What Chime Biologics does

Chime Biologics is a privately held biologics contract development and manufacturing organization (CDMO) founded in 2013 and headquartered in Wuhan, China, with additional operations in Shanghai (China Innovation Hub), Basel (European Innovation Hub opened June 2025), and sales offices in San Diego, Boston, and Paris. The company operates the world's first KUBio modular biopharmaceutical factory built with GE/Cytiva technology, using single-use bioreactors at 50L, 200L, 500L, and 2000L cGMP scales to manufacture monoclonal antibodies, bispecific antibodies, fusion proteins, conjugated proteins, enzymes, and vaccines. Its facilities are designed to meet NMPA, EMA, US FDA, and EU PIC/S GMP standards, and the company reports more than 70 successful 2000L GMP production batches and clinical material supply to clients across 30+ countries.

The company's service portfolio spans the full biologics development lifecycle: cell line development, process development, protein science, technology transfer, drug substance manufacturing, drug product manufacturing (including liquid fill, lyophilized fill and pre-filled syringe fill in isolators), quality systems, regulatory support, project management, and data integrity. In November 2025 it launched the Chime AI Platform in partnership with Opq Therapeutics, adding AI-enabled target screening, antibody design and optimization, AI-enhanced cell line development, and AI-integrated rapid CMC as adjacent offerings. The business operates on professional-services contracts with biotech and biopharmaceutical clients, priced project-by-project, and pursues co-development and strategic partnerships (e.g., Polpharma Biologics, SunRock Biopharma, Domain Therapeutics, Daewoong Pharmaceutical, Libang Pharmaceuticals, TNAX Biopharma) as a parallel go-to-market channel.

Chime generates revenue through negotiated CDMO contracts and strategic collaborations with global biotech and biopharmaceutical clients. Pricing is quote-based and varies with scope, scale and development stage, typical of the contract manufacturing industry. The company is scaling aggressively: a US$190 million Series A+ in May 2024 (led by VMS Group with Fidelity International and Panacea Venture) and a December 2025 Optics Valley Financial Holdings round are funding capacity expansion toward 140,000+ liters over five years, while the Chime Innovation Alliance and Basel hub extend its commercial reach across China, Europe, and APAC.

Chime Biologics firmographics

Firmographics
Name
Chime Biologics
Legal name
Chime Biologics (Wuhan) Co., Ltd.
Website
https://chimebiologics.com
Company type
Private
Founded year
2013
Operating status
Operating
Headcount range
501–1,000 employees
Short description
Chime Biologics is a privately held Chinese CDMO providing end-to-end biologics development and manufacturing — from cell line development through commercial drug substance and drug product supply — serving global biotech and pharmaceutical clients across 30+ countries via its Wuhan KUBio modular facility and Basel European Innovation Hub.
Ownership category
akta.pro rank

Chime Biologics industry classification

Industry
Product category
Biopharmaceutical Contract Manufacturing (CDMO)
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Pharmaceutical Preparation Manufacturing (325412)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Biologics (mAbs/Recombinant Proteins) CDMO (HLAGABAC)
akta.pro secondary industries
Biologic API/Drug Substance Manufacturing Services (HLAAAKAA), Process Development & Tech Transfer Services (upstream/downstream) (HLAAAKAF), Sterile Fill-Finish & Aseptic Manufacturing CDMO (HLAGABAH)

Keywords

  • Biologics contract manufacturing
  • CDMO services
  • Drug substance manufacturing
  • Cell line development
  • Biopharmaceutical development

Where Chime Biologics is headquartered

Location

Headquarters

HQ city
Wuhan
HQ country
China
HQ region
Asia

Offices6 records

Markets served

Chime Biologics business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Infrastructure, Technology or R&D, Operations, Supply Chain, Marketing or Sales

Revenue model

  1. CDMO Contract Manufacturing Services: Full-suite contract development and manufacturing organization (CDMO) services including cell line development, process development, protein science, technology transfer, drug substance manufacturing, drug product manufacturing, quality control/assurance, regulatory support, and project management. Revenue generated through service contracts and manufacturing agreements with biotech and pharmaceutical clients across the development lifecycle from preclinical through commercial stages.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels5 records

Chime Biologics product offering

Product offering

Core offering

Chime Biologics is a global Contract Development and Manufacturing Organization (CDMO) that provides end-to-end biologics manufacturing services for biotech and pharmaceutical companies. The company offers services spanning cell line development, process development, drug substance manufacturing (50L–2000L), drug product manufacturing, technology transfer, quality control, and regulatory support from pre-clinical through commercial stages. Its operations leverage the world's first GE KuBio modular biopharmaceutical manufacturing facility using single-use bioprocessing technology, complemented by the newly launched Chime AI Platform for AI-driven biologics discovery and development.

Product overview

Chime Biologics is a leading global CDMO (Contract Development and Manufacturing Organization) providing end-to-end biologics manufacturing services from pre-clinical support through clinical and commercial manufacturing. The portfolio consists of core service modules including Cell Line Development, Process Development, Protein Science Group, Technology Transfer, Drug Substance Manufacturing (M-DS), Drug Product Manufacturing (M-DP), Quality System, Regulatory Support, Project Management, and Data Integrity. These services are powered by key technology platforms: the KUBio modular biopharmaceutical factory (world's first modular facility using single-use bioreactors from GE/Cytiva), and the Chime AI Platform for AI-driven biologics development. Manufacturing capabilities span scales from 50L to 2000L bioreactors for diverse molecule types including monoclonal antibodies, bispecific antibodies, fusion proteins, conjugated proteins, enzymes, and vaccines.

Differentiator

Problem solved

Functional benefit

Products and services

  • End-to-End CDMO Services

Quantifiable outcome

  • Successfully completed over 70 batches of 2000L GMP production
  • +2 more outcomes

Companies that use Chime Biologics

Customer profile

Named customers1 record

Segments2 records

Ideal customer profiles2 records

Chime Biologics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability4 records

Feature7 records

Chime Biologics partnerships and signals

Strategic signal

Partnerships

Ten partnerships are on record, tiered major, regional, strategic, core and supporting.

  • Beijing Libang Pharmaceutical (Libang Pharmaceuticals)majorStrategic or Co-development Partner · 10 December 2025Strategic collaboration to develop a biosimilar to Amgen's Blincyto (blinatumomab) for global markets. Chime Biologics will leverage its GMP manufacturing platform and regulatory expertise to support the biosimilar development program.
  • TNAX BiopharmaregionalStrategic or Co-development Partner · 9 December 2025Strategic collaboration marking Chime Biologics' first partnership in Japan. TNAX Biopharma is a Japanese biotech company.
  • Opq Therapeutics (奥泊生科)strategicTechnology or Integration · 2 November 2025Strategic collaboration on AI-driven biologics discovery. Opq provides advanced AI technology for target screening, antibody design, and optimization while Chime provides CMC capabilities. Co-founders include Nobel Laureate Michael Levitt.
  • SunRock BiopharmamajorStrategic or Co-development Partner · 21 October 2025Strategic collaboration to develop SRB5, a novel anti-CCR9 monoclonal antibody targeting inflammatory bowel disease (IBD) with potential expansion into other immune-mediated inflammatory indications. SunRock Biopharma is a Spanish biotech company focused on next-generation therapeutic antibodies.
  • Superlab SuissecoreTechnology or Integration · 6 June 2025Host facility for Chime Biologics' European Innovation Hub in Basel. Superlab Suisse provides laboratory space and infrastructure enabling Chime's operations in the heart of Europe's biotech ecosystem.
  • Basel Area Business and InnovationsupportingStrategic or Co-development Partner · 6 June 2025Basel Area Business and Innovation is the official economic development agency for the Basel area. They support and promote the biotech ecosystem and welcomed Chime Biologics' establishment of European Innovation Hub in Basel.
  • Chime Innovation Alliance PartnerscoreStrategic or Co-development Partner · 6 June 2025Alliance of leading Chinese biotech service providers providing one-stop solutions for customers from drug discovery through preclinical, clinical, and commercial stages. Partner companies include Sepax Bioscience, AnLing, Alioth Biotech, NanoMicro, Duoning Biotech, Lisure, and others.
  • Japan-China Bio-Innovation Ecosystem Forum PartnerssupportingStrategic or Co-development Partner · 22 May 2025Co-organized with Duoning Biotech and Lisure to promote innovation, collaboration, and investment between Japan and China in the biopharmaceutical industry.
  • Polpharma BiologicsmajorStrategic or Co-development Partner · 16 April 2025Strategic partnership with Poland-based Polpharma Biologics to support end-to-end development and manufacture of a biosimilar product for the global market. Chime provides integrated support from IND stage through commercial supply. Polpharma has two biosimilars approved by FDA and EMA.
  • Domain TherapeuticsmajorStrategic or Co-development Partner · 12 March 2024Manufacturing agreement for DT-7012, a novel anti-CCR8 antibody for cancer immunotherapy. Chime provides cell line development, process development, scale-up, and Phase I GMP clinical manufacturing. DT-7012 is a potential best-in-class Treg-depleting antibody.

Scale indicators6 records

Recent moves7 records

Expansion highlights6 records

Chime Biologics competitors and assessment

Company assessment

Broad incumbents

  • Lonza: Swiss-based global CDMO with extensive biologics manufacturing capabilities across mammalian and microbial platforms. Serves as the dominant Western incumbent in biologics CDMO, competing with Chime for large-pharma and biotech contracts across multiple regulatory jurisdictions.
  • Catalent: Large US-headquartered CDMO with biologics fill-finish, cell line, and biomanufacturing capabilities as part of a broader services portfolio. Overlaps with Chime on biologics drug substance and drug product manufacturing while also serving injectables, oral, and inhalation delivery.

Direct peers

  • Samsung Biologics: Korean-based global biologics CDMO with large-scale cGMP manufacturing capacity (expanding toward ~1M liters) and full lifecycle services from clinical to commercial supply. Direct competitor for global biotech CDMO contracts with overlapping mAb and bispecific capabilities.
  • WuXi Biologics: China-headquartered, Hong Kong-listed global biologics CDMO offering end-to-end services from cell line development through commercial manufacturing. The most direct competitor to Chime Biologics in terms of geographic origin, service portfolio, and target customer base, with materially larger scale (~600,000L capacity).
  • AGC Biologics: Global biologics CDMO with manufacturing sites in the US, Europe, and Japan, offering mammalian and microbial-based biologics development and manufacturing services. Comparable mid-large tier peer competing for similar global biotech CDMO engagements.
  • Bora Pharmaceuticals: Taiwan-headquartered CDMO with rapidly expanding biologics manufacturing capabilities alongside its established small-molecule franchise. Emerging direct competitor in Asia-Pacific biologics CDMO space with similar growth-oriented capacity expansion trajectory.
  • KBI Biopharma: US-headquartered biologics CDMO (acquired by JSR Life Sciences) offering process development, analytical services, and cGMP manufacturing. Comparable mid-tier peer with similar focus on mammalian cell-based biologics and competitive pressure in the same customer segment.
  • Boehringer Ingelheim BioXcellence: German-headquartered biologics CDMO division of Boehringer Ingelheim offering contract manufacturing from cell line through commercial supply. Direct peer with comparable service portfolio and similar positioning in mammalian-cell biologics manufacturing for global biotech clients.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights6 records

Customer concentration

Chime Biologics social profiles

Digital presence

Chime Biologics compliance and trust

Trust signal

Compliance6 records

Chime Biologics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Chime Biologics leadership team

Management profile

Number of profiles

Profiles4 records

Chime Biologics funding detail

Funding detail

Funding overview

Funding rounds4 records

Investors5 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Chime Biologics M&A and investment

M&A and investment

M&A

Investments1 record

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Chime Biologics

What does Chime Biologics do?

Chime Biologics is a global Contract Development and Manufacturing Organization (CDMO) that provides end-to-end biologics manufacturing services for biotech and pharmaceutical companies. The company offers services spanning cell line development, process development, drug substance manufacturing (50L–2000L), drug product manufacturing, technology transfer, quality control, and regulatory support from pre-clinical through commercial stages. Its operations leverage the world's first GE KuBio modular biopharmaceutical manufacturing facility using single-use bioprocessing technology, complemented by the newly launched Chime AI Platform for AI-driven biologics discovery and development.

Is Chime Biologics a public or private company?

Chime Biologics is a private company. It is classified as venture growth investor backed and is currently operating.

When was Chime Biologics founded?

Chime Biologics was founded in 2013. It employs 501 to 1,000 people.

Where is Chime Biologics based?

Chime Biologics is headquartered in Wuhan, China, in the Asia region.

How does Chime Biologics make money?

One revenue line is on record: CDMO Contract Manufacturing Services.

Who are Chime Biologics's main competitors?

Broad incumbents on record are Lonza and Catalent. Direct peers are Samsung Biologics, WuXi Biologics, AGC Biologics, Bora Pharmaceuticals, KBI Biopharma and Boehringer Ingelheim BioXcellence.

Does Chime Biologics have an API?

No public API is recorded for Chime Biologics.

What industry is Chime Biologics in?

Chime Biologics's product category is Biopharmaceutical Contract Manufacturing (CDMO). Its primary akta.pro industry code is HLAGABAC, Biologics (mAbs/Recombinant Proteins) CDMO, with a secondary code of HLAAAKAA, Biologic API/Drug Substance Manufacturing Services. Its NAICS code is 541714 and its SIC code is 8731.

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Live signals
YahooInside the USD 52.23B Transformation of Biosimilar Contract Manufacturing by 2035A market report published by Towards Healthcare projects the global biosimilar contract manufacturing market will grow from USD 9.22 billion in 2025 to approximately USD 52.23 billion by 2035, representing an 18.94% CAGR during the forecast period. Key recent developments include strategic partnerships and investments by Chime Biologics, Polpharma Biologics, Celltrion, and Sandoz expanding global manufacturing capacity for biosimilars, with the oncology segment expected to grow at the fastest rate. The report identifies regulatory complexity, compliance costs, and technology transfer risks as emerging challenges facing the sector.BioSpaceSunRock Biopharma and Chime Biologics Announce Strategic Collaboration to Advance Development of Anti-CCR9 Antibody SRB5SunRock Biopharma, a Spanish biotechnology company, and Chime Biologics, a global contract development and manufacturing organization (CDMO) based in China, have announced a strategic collaboration to develop SRB5, a novel anti-CCR9 monoclonal antibody targeting inflammatory bowel disease. Chime Biologics will provide its global-standard GMP manufacturing platform to scale production and accelerate preclinical and regulatory milestones for the antibody. The collaboration is positioned as a critical step toward clinical validation of SRB5, which has potential applications in Crohn's disease, ulcerative colitis, and potentially in CCR9-expressing tumors.Business Wire BlogSunRock Biopharma and Chime Biologics Announce Strategic Collaboration to Advance Development of Anti-CCR9 Antibody SRB5SunRock Biopharma and Chime Biologics announced a strategic collaboration to advance SRB5, a humanized anti-CCR9 monoclonal antibody for inflammatory bowel disease. The partnership leverages Chime's GMP manufacturing platform to scale production and accelerate preclinical and regulatory milestones. SRB5 targets CCR9+ cells involved in chronic intestinal inflammation.The Pharma LetterChime and Polpharma strike deal on global biosimilar developmentChina's Chime Biologics has formed a strategic partnership with Poland-based Polpharma Biologics to support the end-to-end development and manufacture of a biosimilar product for the global market. The deal, announced on April 16, will see Chime provide integrated support from investigational new drug stage through to commercial supply, though the companies did not disclose the specific therapy or target indication. Polpharma, Poland's largest biotech firm, already has two biosimilars approved by both the US FDA and European Medicines Agency, with a pipeline spanning early- and late-stage programs.PR NewswireChime Biologics and Mabgeek Achieve MG-K10 PPQ Milestone, Advancing Atopic Dermatitis and Asthma Therapies Antibody Drug MG-K10 Late-Stage Clinical Trials and CommercializationChime Biologics and Mabgeek announced the successful completion of Process Performance Qualification (PPQ) for MG-K10, a humanized anti-IL-4Rα monoclonal antibody targeting Th2-mediated inflammatory diseases including atopic dermatitis, asthma, and COPD. The PPQ milestone validates manufacturing standards and regulatory compliance, advancing the therapy toward Phase III clinical trials and commercial manufacturing. The companies are strategically focused on entering the American and European markets with what they claim is the world's first once-monthly dosing IL-4Rα-targeting antibody therapeutic.PR NewswireChime Biologics and Korean Listed Company MedPacto Form Strategic Partnership to Accelerate Global Biologics Development and ManufacturingChime Biologics, a leading global CDMO, announced a strategic collaboration with MedPacto, a South Korean KOSDAQ-listed cancer therapeutics company, to advance the CMC process development for MedPacto's preclinical drug candidates and enable streamlined clinical manufacturing for IND submissions. Under the agreement, Chime Biologics will leverage its expertise in biologics development to support MedPacto's expansion into major global markets. Chime Biologics is simultaneously expanding its manufacturing capacity to 100,000 liters as part of its strategy to establish a stronger presence in the South Korean biopharmaceutical market.ChimebiologicsChime Biologics Announced the Completion of US$190 Million Series A+ Financing to Accelerate Capacity ExpansionChime Biologics has secured a total commitment of US$190 million in Series A+ financing, with over $100 million closed immediately, to accelerate its capacity expansion. The investment round was led by VMS Group and included participation from Fidelity International and Panacea Venture. These funds will support the construction of Phase II of its facility in Wuhan, aiming to increase manufacturing capacity to more than 140,000 liters within five years.PR NewswireChime Biologics and Hope Medicine Enter Manufacturing Agreement to Speed up the Launch of First-in-class Antibody Drug HMI-115 Targeting Endometriosis and Androgenic AlopeciaChime Biologics and Hope Medicine announced a manufacturing agreement on September 28, 2023, for the development and production of HMI-115, a first-in-class monoclonal antibody targeting endometriosis and androgenetic alopecia. Under the agreement, Chime Biologics will provide end-to-end CMC services including technology transfer, process optimization, Phase III GMP production, and commercial manufacturing, while Hope Medicine will leverage Chime's experience in late-stage development and BLA filings to accelerate the drug's clinical advancement and market entry. HMI-115 has received regulatory approvals for Phase II trials in the US, Europe, and China, with global rights owned by Hope Medicine under an exclusive license agreement with Bayer AG signed in 2019.PR NewswireChime Biologics Announced Global Strategic Cooperation with Panolos Bioscience to Advance Multi-specific Therapeutic Proteins DevelopmentChime Biologics and Panolos Bioscience signed a global strategic collaboration agreement on September 19, 2023, in Wuhan, China, to develop PB203, a next-generation multi-specific immuno-oncology drug targeting solid tumors including pancreatic cancer. Under the agreement, Chime Biologics will provide end-to-end CMC solutions including cell line development, process development, and GMP manufacturing using its proprietary CHOrus platform for Panolos Bioscience's PB203, which is currently in preclinical stage with plans to enter US Phase I clinical trials. The collaboration marks Chime Biologics' expansion into global markets and represents a cross-border China-South Korea partnership in advanced biologics development.PR NewswireChime Biologics Announces Strategic Cooperation with Leads Biolabs and BeiGene to Advance LBL-007 mAb Development and Manufacturing GloballyChime Biologics has established a strategic three-way cooperation with Leads Biolabs and BeiGene to accelerate the global development and manufacturing of LBL-007, a novel anti-LAG-3 monoclonal antibody. This partnership involves Chime providing IND filing support and clinical trial materials in China for Leads Biolabs, while also supporting overseas IND applications and clinical supply for BeiGene. The collaboration aims to expedite the progression of LBL-007 through Phase II clinical trials across multiple indications including melanoma and solid tumors.