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Sundia MediTech

Full company profile

uuid000kqg9

Namestring
Sundia MediTech
Legal namestring
BioDuro
Websiteurl
sundia.com
Company typeenum
Private
Founded yearint
1996
Descriptiontext

BioDuro (operating brand of Sundia MediTech) is a fully integrated Contract Research, Development, and Manufacturing Organization (CRDMO) providing end-to-end pharmaceutical services from drug discovery through commercial manufacturing. Founded in 1996 and headquartered in Irvine, California, with a global footprint across 8 campuses, BioDuro operates as a platform-plus-modules architecture built on three service pillars—Discovery (chemistry, DMPK, biology), Drug Substance (process R&D, scale-up synthesis, API manufacturing), and Drug Product (preformulation, formulation, commercial manufacturing). The company supports specialized technology platforms for emerging modalities including Antibody-Drug Conjugates (ADC), PROTAC, DNA-Encoded Library screening, peptide chemistry, and NASH/MASH preclinical models. IND-enabling services span FDA, NMPA, and other major regulatory jurisdictions.

The company serves over 1,500 active customers globally, primarily pharmaceutical and biotechnology companies ranging from large pharma to clinical-stage biotech, with academic and research institutions as a secondary segment. BioDuro employs 2,000+ scientists worldwide according to its website, while firmographic records for the Sundia MediTech entity indicate 501-1,000 employees (suggesting the broader global workforce operates across affiliated entities). The revenue model is contract-based fee-for-service with multi-year project engagements, custom-quoted by scope, duration, and complexity. GTM is enterprise field sales targeting pharmaceutical R&D leadership and procurement directly, supplemented by industry events, scientific webinars, and content marketing.

Disclosed funding history for Sundia MediTech totals $10.5M across a 2005 seed/Series A round from IDG Capital ($2.5M) and a 2008 Series B led by AsiaVest Partners and IDG Capital ($8M), with a 2015 undisclosed investment from Darwin Venture Management. No parent company is disclosed, but the website references 'Our Investors,' confirming institutional backing. Recent activity includes strategic partnerships with CTI Biotechnology (April 2026) and Gilva Therapeutics (May 2026), along with scientific advisory appointments of Dr. Andrew Thomas and Dr. Stevan Djuric (March 2026). CEO is Jim Li. BioDuro marked its 30th anniversary with a Shanghai symposium in June 2025 under the theme 'Accelerating Breakthroughs Through Innovation.'

Short descriptiontext

BioDuro (Sundia MediTech) is a fully integrated CRDMO providing end-to-end drug discovery, development, and manufacturing services across 8 global campuses with 2,000+ scientists, serving over 1,500 pharmaceutical and biotechnology customers worldwide.

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

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
contract research services, drug discovery services, preclinical development, pharmaceutical manufacturing, biotechnology CRO
Industry4 codes
1HLAGAFAC
CodeHLAGAFACPrimaryNo
2HLAGAAAL
CodeHLAGAAALPrimaryNo
3HLAGABAK
CodeHLAGABAKPrimaryNo
4HLAGAHAL
CodeHLAGAHALPrimaryNo
NAICS code4 codes
  • 5417
  • 541714
  • 3254
  • 325412
SIC code3 codes
  • 8731
  • 2834
  • 8071
Product category
Contract Research and Development Services
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model3 records
1Contract Research and Development Services
TypeProfessional Services
Description

Fee-for-service model providing drug discovery and development services including chemistry, DMPK, biology, and preclinical studies. Revenue generated through project-based contracts with pharmaceutical and biotechnology companies.

bioduro.com
2Drug Substance Manufacturing
TypeOne Time License
Description

Manufacturing services for APIs, RSMs, and intermediates at kilo and pilot scale, including scale-up synthesis and IND enabling capabilities for FDA, NMPA and other regulatory filings.

bioduro.com
3Drug Product Development and Manufacturing
TypeOne Time License
Description

Formulation development, analytical services, and manufacturing for solid oral dosage forms from clinical through commercial stages.

bioduro.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components5 values
Personnel, Operations, Infrastructure, Technology or R&D, Marketing or Sales
Pricing details1 tier
1Quote-based project pricing
ModelOtherBilling cadenceMulti-year contract
Notes

CRO/CDMO services are custom quoted based on project scope, service types, timeline, and volume requirements

bioduro.com
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 record
1Solution Engine
Description

Tailored engine for small molecular drug discovery, unlocking exponential possibilities screening billions of small molecules.

bioduro.com
Core offering1 text field

Sundia MediTech is a Contract Research, Development and Manufacturing Organization (CRDMO) that provides integrated drug discovery and development services to pharmaceutical and biotechnology companies worldwide. The company delivers end-to-end capabilities spanning Discovery (Chemistry, DMPK, Biology), Drug Substance manufacturing, and Drug Product development, supported by specialized platforms for antibody-drug conjugates, peptides, PROTAC, DNA-encoded libraries, and disease-specific preclinical models.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • Accelerated breakthroughs through integrated innovation
Product overview1 text field

Sundia MediTech (operating as BioDuro) is a fully integrated Global CRDMO (Contract Research, Development, and Manufacturing Organization) providing end-to-end pharmaceutical and biotechnology research services. The company operates as a platform-plus-modules architecture with three core service pillars (Discovery, Drug Substance, Drug Product) supported by specialized platforms including Antibody-Drug Conjugate, Peptide, PROTAC, DNA-Encoded Library (DEL), Integrated Drug Discovery, Solution Engine, IND Enabling, NASH Mouse Models, and Compound Management. The unified platform approach enables seamless integration from target identification through preclinical candidate selection to IND filing, serving over 1,500 active customers globally across 8 campuses with 2,000+ scientists. BioDuro was founded in 1996 and is headquartered in Irvine, CA.

Product and service14 records
1Discovery Services
CategoryDrug Discovery
Description

Comprehensive drug discovery services covering Chemistry (peptide chemistry, medicinal chemistry, computational chemistry, synthetic chemistry, analytical chemistry, scale-up chemistry, fragment-based drug discovery), DMPK (in vivo PK/TK, in vitro ADME, bioanalytical services, toxicity studies, large molecule development), and Biology (assay development, biochemical and cellular assays, ligand binding assays, protein science, SPR biophysics, biologics) for pharmaceutical and biotechnology clients.

2Drug Substance Services
CategoryDrug Substance Manufacturing
Description

End-to-end drug substance services including process R&D (flow chemistry, sugar chemistry, peptide chemistry, preparative purification, process safety assessment), scale-up synthesis, and drug substance manufacturing at kilo and pilot scale for APIs, RSMs, and intermediates, with QA and EHS support for pharmaceutical clients.

3Drug Product Services
CategoryDrug Product Development
Description

Drug product development services including preformulation, formulation development (hot melt extrusion, spray dried dispersion, amorphous solid dispersion, bioavailability enhancement, modified release), analytical services, and drug product manufacturing for clinical and commercial stages, serving pharmaceutical and biotechnology companies.

4Oncology Services
CategorySpecialized Biology Services
Description

Preclinical oncology research services including PDX (patient-derived xenograft), CDX (cell-derived xenograft), orthotopic models, syngeneic models, humanized mouse models, CAR-T and CAR-NK mouse models, ELISA assays, and in vitro assays for oncology drug developers.

5Pharmacology Services
CategorySpecialized Biology Services
Description

Preclinical pharmacology services covering immunology and inflammation, metabolic disorders, MASH/NASH mouse models, respiratory diseases, neuroscience, and safety pharmacology for drug developers across therapeutic areas.

6Antibody-Drug Conjugate Platform
CategorySpecialized Platform
Description

Specialized platform for antibody-drug conjugate (ADC) development and manufacturing services supporting pharmaceutical and biotechnology clients working on targeted cancer therapeutics.

7Peptide Platform
CategorySpecialized Platform
Description

Comprehensive peptide chemistry platform for peptide drug discovery and development, including custom peptide synthesis and scale-up services for pharmaceutical and biotechnology companies.

8PROTAC Platform
CategorySpecialized Platform
Description

PROTAC (Proteolysis-Targeting Chimera) technology platform for targeted protein degradation drug discovery, enabling pharmaceutical and biotechnology clients to develop therapies against previously undruggable targets.

9DNA-Encoded Library (DEL) Platform
CategorySpecialized Platform
Description

DNA-encoded library technology platform for high-throughput screening of billions of small molecules for hit generation, supporting accelerated lead discovery for pharmaceutical and biotechnology clients.

10Integrated Drug Discovery Platform
CategoryIntegrated Platform
Description

Fully integrated drug discovery platform providing comprehensive services from target identification to preclinical candidate compound (PCC), combining synthetic chemistry, biology, DMPK, and other disciplines under one roof for pharmaceutical and biotechnology clients.

11Solution Engine
CategorySpecialized Platform
Description

Tailored engine for small molecular drug discovery enabling screening of billions of small molecules with exponential possibilities for hit identification and lead optimization by pharmaceutical and biotechnology clients.

12IND Enabling Services
CategoryRegulatory Services
Description

IND (Investigational New Drug) enabling services to support regulatory filings with FDA, NMPA, and other major agencies for pharmaceutical and biotechnology companies advancing candidates to clinical trials.

13MASH/NASH Mouse Models
CategorySpecialized Platform
Description

Advanced preclinical NASH (Metabolic dysfunction-Associated SteatoHepatitis) mouse models providing clinical relevance with shortened timelines for metabolic disease drug developers.

14Compound Management
CategorySpecialized Platform
Description

Automated, flexible, and customized compound management platform for efficient handling and storage of chemical compounds during drug discovery for pharmaceutical and biotechnology clients.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-04-28
Description

BioDuro and CTI Biotechnology entered a strategic partnership to accelerate preclinical drug development. This collaboration leverages BioDuro's integrated CRDMO capabilities with CTI Biotechnology's expertise to provide comprehensive preclinical development solutions for clients.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

BioDuro congratulated Gilva Therapeutics on advancing GV-100 into Phase I Clinical Development in Australia, indicating an ongoing partnership supporting the client's clinical advancement program.

Recent move5 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Mid-sized clinical CRO serving biotech/small pharma. Comparable customer segment and quality reputation, but concentrated in clinical rather than preclinical discovery.

TypeBroad incumbent
Description

Global CRO focused on clinical development with growing lab/biomarker services. Partial overlap with BioDuro on early development and bioanalytical services through its PRA Health combination.

TypeDirect peer
Description

China-headquartered, fully integrated CRDMO offering discovery, manufacturing, and clinical services globally. Direct competitor with overlapping one-stop-shop positioning, comparable China footprint, and similar breadth across modalities including ADC and PROTAC.

TypeBroad incumbent
Description

Global clinical and commercial CRO. Overlaps BioDuro on biotech client base and drug development services though weighted toward clinical operations.

TypeBroad incumbent
Description

Largest global CRO with full clinical and R&D services portfolio plus data/technology capabilities. Overlaps BioDuro on preclinical and lab services as a broader portfolio player.

TypeDirect peer
Description

Global preclinical CRO/CDMO with strong discovery, safety assessment, and biologics manufacturing franchises. Directly comparable in preclinical CRO, DMPK, and biologics capabilities though with a heavier US/EU footprint.

TypeDirect peer
Description

China-rooted, UK-/US-extended CRDMO providing laboratory, CMC, and biologics services. Closest comparable in operating model (China cost base + US/UK delivery) and end-to-end discovery-to-manufacturing scope.

TypeDirect peer
Description

China-headquartered clinical and preclinical CRO serving global pharma and biotech. Comparable in target customer base and China-based delivery, with growing discovery CRO capability similar to BioDuro.

TypeDirect peer
Description

US-listed CRO/CDMO with integrated lab and CMC services and significant China operations. Comparable in discovery bioanalytical, DMPK, and drug substance scope.

TypeBroad incumbent
Description

Major US clinical/preclinical CRO with global lab services. Comparable in early development CRO and bioanalytical offerings, though oriented more toward clinical scale.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers2 records

Each record includes

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

Segment3 records

Each record includes

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

Ideal customer profile3 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
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature10 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles1 record

Each record includes

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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

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

Investors3 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

Investment

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 →

Sundia MediTech

Contract Research and Development Servicessundia.com

BioDuro (Sundia MediTech) is a fully integrated CRDMO providing end-to-end drug discovery, development, and manufacturing services across 8 global campuses with 2,000+ scientists, serving over 1,500 pharmaceutical and biotechnology customers worldwide.

What Sundia MediTech does

BioDuro (operating brand of Sundia MediTech) is a fully integrated Contract Research, Development, and Manufacturing Organization (CRDMO) providing end-to-end pharmaceutical services from drug discovery through commercial manufacturing. Founded in 1996 and headquartered in Irvine, California, with a global footprint across 8 campuses, BioDuro operates as a platform-plus-modules architecture built on three service pillars—Discovery (chemistry, DMPK, biology), Drug Substance (process R&D, scale-up synthesis, API manufacturing), and Drug Product (preformulation, formulation, commercial manufacturing). The company supports specialized technology platforms for emerging modalities including Antibody-Drug Conjugates (ADC), PROTAC, DNA-Encoded Library screening, peptide chemistry, and NASH/MASH preclinical models. IND-enabling services span FDA, NMPA, and other major regulatory jurisdictions.

The company serves over 1,500 active customers globally, primarily pharmaceutical and biotechnology companies ranging from large pharma to clinical-stage biotech, with academic and research institutions as a secondary segment. BioDuro employs 2,000+ scientists worldwide according to its website, while firmographic records for the Sundia MediTech entity indicate 501-1,000 employees (suggesting the broader global workforce operates across affiliated entities). The revenue model is contract-based fee-for-service with multi-year project engagements, custom-quoted by scope, duration, and complexity. GTM is enterprise field sales targeting pharmaceutical R&D leadership and procurement directly, supplemented by industry events, scientific webinars, and content marketing.

Disclosed funding history for Sundia MediTech totals $10.5M across a 2005 seed/Series A round from IDG Capital ($2.5M) and a 2008 Series B led by AsiaVest Partners and IDG Capital ($8M), with a 2015 undisclosed investment from Darwin Venture Management. No parent company is disclosed, but the website references 'Our Investors,' confirming institutional backing. Recent activity includes strategic partnerships with CTI Biotechnology (April 2026) and Gilva Therapeutics (May 2026), along with scientific advisory appointments of Dr. Andrew Thomas and Dr. Stevan Djuric (March 2026). CEO is Jim Li. BioDuro marked its 30th anniversary with a Shanghai symposium in June 2025 under the theme 'Accelerating Breakthroughs Through Innovation.'

Sundia MediTech firmographics

Firmographics
Name
Sundia MediTech
Legal name
BioDuro
Website
https://sundia.com
Company type
Private
Founded year
1996
Operating status
Operating
Headcount range
501–1,000 employees
Short description
BioDuro (Sundia MediTech) is a fully integrated CRDMO providing end-to-end drug discovery, development, and manufacturing services across 8 global campuses with 2,000+ scientists, serving over 1,500 pharmaceutical and biotechnology customers worldwide.
Ownership category
akta.pro rank

Where Sundia MediTech is headquartered

Location

Headquarters

HQ city
Shanghai
HQ country
China
HQ region
Asia

Offices3 records

Markets served

Sundia MediTech business model

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

Revenue model

  1. Contract Research and Development Services: Fee-for-service model providing drug discovery and development services including chemistry, DMPK, biology, and preclinical studies. Revenue generated through project-based contracts with pharmaceutical and biotechnology companies.
  2. Drug Substance Manufacturing: Manufacturing services for APIs, RSMs, and intermediates at kilo and pilot scale, including scale-up synthesis and IND enabling capabilities for FDA, NMPA and other regulatory filings.
  3. Drug Product Development and Manufacturing: Formulation development, analytical services, and manufacturing for solid oral dosage forms from clinical through commercial stages.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractQuote-based project pricing

Go-to-market motion1 record

Distribution channels1 record

Marketing channels6 records

Sundia MediTech product offering

Product offering

Core offering

Sundia MediTech is a Contract Research, Development and Manufacturing Organization (CRDMO) that provides integrated drug discovery and development services to pharmaceutical and biotechnology companies worldwide. The company delivers end-to-end capabilities spanning Discovery (Chemistry, DMPK, Biology), Drug Substance manufacturing, and Drug Product development, supported by specialized platforms for antibody-drug conjugates, peptides, PROTAC, DNA-encoded libraries, and disease-specific preclinical models.

Product overview

Sundia MediTech (operating as BioDuro) is a fully integrated Global CRDMO (Contract Research, Development, and Manufacturing Organization) providing end-to-end pharmaceutical and biotechnology research services. The company operates as a platform-plus-modules architecture with three core service pillars (Discovery, Drug Substance, Drug Product) supported by specialized platforms including Antibody-Drug Conjugate, Peptide, PROTAC, DNA-Encoded Library (DEL), Integrated Drug Discovery, Solution Engine, IND Enabling, NASH Mouse Models, and Compound Management. The unified platform approach enables seamless integration from target identification through preclinical candidate selection to IND filing, serving over 1,500 active customers globally across 8 campuses with 2,000+ scientists. BioDuro was founded in 1996 and is headquartered in Irvine, CA.

Differentiator

Problem solved

Functional benefit

Brands

  • Solution Engine: Tailored engine for small molecular drug discovery, unlocking exponential possibilities screening billions of small molecules.

Products and services

  • Discovery Services Comprehensive drug discovery services covering Chemistry (peptide chemistry, medicinal chemistry, computational chemistry, synthetic chemistry, analytical chemistry, scale-up chemistry, fragment-based drug discovery), DMPK (in vivo PK/TK, in vitro ADME, bioanalytical services, toxicity studies, large molecule development), and Biology (assay development, biochemical and cellular assays, ligand binding assays, protein science, SPR biophysics, biologics) for pharmaceutical and biotechnology clients.
  • Drug Substance Services End-to-end drug substance services including process R&D (flow chemistry, sugar chemistry, peptide chemistry, preparative purification, process safety assessment), scale-up synthesis, and drug substance manufacturing at kilo and pilot scale for APIs, RSMs, and intermediates, with QA and EHS support for pharmaceutical clients.
  • Drug Product Services Drug product development services including preformulation, formulation development (hot melt extrusion, spray dried dispersion, amorphous solid dispersion, bioavailability enhancement, modified release), analytical services, and drug product manufacturing for clinical and commercial stages, serving pharmaceutical and biotechnology companies.
  • Oncology Services Preclinical oncology research services including PDX (patient-derived xenograft), CDX (cell-derived xenograft), orthotopic models, syngeneic models, humanized mouse models, CAR-T and CAR-NK mouse models, ELISA assays, and in vitro assays for oncology drug developers.
  • Pharmacology Services Preclinical pharmacology services covering immunology and inflammation, metabolic disorders, MASH/NASH mouse models, respiratory diseases, neuroscience, and safety pharmacology for drug developers across therapeutic areas.
  • Antibody-Drug Conjugate Platform Specialized platform for antibody-drug conjugate (ADC) development and manufacturing services supporting pharmaceutical and biotechnology clients working on targeted cancer therapeutics.
  • Peptide Platform Comprehensive peptide chemistry platform for peptide drug discovery and development, including custom peptide synthesis and scale-up services for pharmaceutical and biotechnology companies.
  • PROTAC Platform PROTAC (Proteolysis-Targeting Chimera) technology platform for targeted protein degradation drug discovery, enabling pharmaceutical and biotechnology clients to develop therapies against previously undruggable targets.
  • DNA-Encoded Library (DEL) Platform DNA-encoded library technology platform for high-throughput screening of billions of small molecules for hit generation, supporting accelerated lead discovery for pharmaceutical and biotechnology clients.
  • Integrated Drug Discovery Platform Fully integrated drug discovery platform providing comprehensive services from target identification to preclinical candidate compound (PCC), combining synthetic chemistry, biology, DMPK, and other disciplines under one roof for pharmaceutical and biotechnology clients.
  • Solution Engine Tailored engine for small molecular drug discovery enabling screening of billions of small molecules with exponential possibilities for hit identification and lead optimization by pharmaceutical and biotechnology clients.
  • IND Enabling Services IND (Investigational New Drug) enabling services to support regulatory filings with FDA, NMPA, and other major agencies for pharmaceutical and biotechnology companies advancing candidates to clinical trials.
  • MASH/NASH Mouse Models Advanced preclinical NASH (Metabolic dysfunction-Associated SteatoHepatitis) mouse models providing clinical relevance with shortened timelines for metabolic disease drug developers.
  • Compound Management Automated, flexible, and customized compound management platform for efficient handling and storage of chemical compounds during drug discovery for pharmaceutical and biotechnology clients.

Quantifiable outcome

  • Accelerated breakthroughs through integrated innovation

Companies that use Sundia MediTech

Customer profile

Named customers2 records

Segments3 records

Ideal customer profiles3 records

Sundia MediTech technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature10 records

Sundia MediTech partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered core.

  • CTI BiotechnologycoreStrategic or Co-development Partner · 28 April 2026BioDuro and CTI Biotechnology entered a strategic partnership to accelerate preclinical drug development. This collaboration leverages BioDuro's integrated CRDMO capabilities with CTI Biotechnology's expertise to provide comprehensive preclinical development solutions for clients.
  • Gilva TherapeuticscoreStrategic or Co-development PartnerBioDuro congratulated Gilva Therapeutics on advancing GV-100 into Phase I Clinical Development in Australia, indicating an ongoing partnership supporting the client's clinical advancement program.

Scale indicators4 records

Recent moves5 records

Expansion highlights4 records

Sundia MediTech competitors and assessment

Company assessment

Broad incumbents

  • Medpace: Mid-sized clinical CRO serving biotech/small pharma. Comparable customer segment and quality reputation, but concentrated in clinical rather than preclinical discovery.
  • ICON plc: Global CRO focused on clinical development with growing lab/biomarker services. Partial overlap with BioDuro on early development and bioanalytical services through its PRA Health combination.
  • Syneos Health: Global clinical and commercial CRO. Overlaps BioDuro on biotech client base and drug development services though weighted toward clinical operations.
  • IQVIA: Largest global CRO with full clinical and R&D services portfolio plus data/technology capabilities. Overlaps BioDuro on preclinical and lab services as a broader portfolio player.
  • Labcorp / Fortrea (Covance spin): Major US clinical/preclinical CRO with global lab services. Comparable in early development CRO and bioanalytical offerings, though oriented more toward clinical scale.

Direct peers

  • WuXi AppTec: China-headquartered, fully integrated CRDMO offering discovery, manufacturing, and clinical services globally. Direct competitor with overlapping one-stop-shop positioning, comparable China footprint, and similar breadth across modalities including ADC and PROTAC.
  • Charles River Laboratories: Global preclinical CRO/CDMO with strong discovery, safety assessment, and biologics manufacturing franchises. Directly comparable in preclinical CRO, DMPK, and biologics capabilities though with a heavier US/EU footprint.
  • Pharmaron: China-rooted, UK-/US-extended CRDMO providing laboratory, CMC, and biologics services. Closest comparable in operating model (China cost base + US/UK delivery) and end-to-end discovery-to-manufacturing scope.
  • Hangzhou Tigermed: China-headquartered clinical and preclinical CRO serving global pharma and biotech. Comparable in target customer base and China-based delivery, with growing discovery CRO capability similar to BioDuro.
  • Frontage Holdings: US-listed CRO/CDMO with integrated lab and CMC services and significant China operations. Comparable in discovery bioanalytical, DMPK, and drug substance scope.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks5 records

Key highlights6 records

Customer concentration

Sundia MediTech social profiles

Digital presence

Sundia MediTech financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Sundia MediTech leadership team

Management profile

Number of profiles

Profiles1 record

Sundia MediTech funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors3 records

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

Sundia MediTech M&A and investment

M&A and investment

M&A

Investments

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

Frequently asked questions about Sundia MediTech

What does Sundia MediTech do?

Sundia MediTech is a Contract Research, Development and Manufacturing Organization (CRDMO) that provides integrated drug discovery and development services to pharmaceutical and biotechnology companies worldwide. The company delivers end-to-end capabilities spanning Discovery (Chemistry, DMPK, Biology), Drug Substance manufacturing, and Drug Product development, supported by specialized platforms for antibody-drug conjugates, peptides, PROTAC, DNA-encoded libraries, and disease-specific preclinical models.

Is Sundia MediTech a public or private company?

Sundia MediTech is a private company. It is classified as venture growth investor backed and is currently operating.

When was Sundia MediTech founded?

Sundia MediTech was founded in 1996. It employs 501 to 1,000 people.

Where is Sundia MediTech based?

Sundia MediTech is headquartered in Shanghai, China, in the Asia region.

How does Sundia MediTech make money?

Three revenue lines are on record. Contract Research and Development Services are the primary driver. The others are drug Substance Manufacturing and drug Product Development and Manufacturing.

Who are Sundia MediTech's main competitors?

Broad incumbents on record are Medpace, ICON plc, Syneos Health, IQVIA and Labcorp / Fortrea (Covance spin). Direct peers are WuXi AppTec, Charles River Laboratories, Pharmaron, Hangzhou Tigermed and Frontage Holdings.

Does Sundia MediTech have an API?

No public API is recorded for Sundia MediTech.

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