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Shanghai Medicilon

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uuid0005c4d

Namestring
Shanghai Medicilon
Legal namestring
Medicilon
Websiteurl
medicilon.com
Company typeenum
Private
Founded yearint
2004
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1,001–5,000
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
preclinical CRO services, drug discovery services, CMC development, IND-enabling studies, safety assessment services
Industry4 codes
1Preclinical CROs (Discovery/Pharmacology/DMPK)
CodeHLAGAAABPrimaryYes
2Toxicology & Safety Assessment CROs (GLP)
CodeHLAGAAACPrimaryNo
3Regulatory Strategy & Global Submissions (IND/CTA/NDA/BLA/MAA)
CodeHLAGAKAAPrimaryNo
4Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC)
CodeHLAGAHAMPrimaryNo
NAICS code3 codes
  • Scientific Research and Development Services5417
  • Research and Development in the Physical, Engineering, and Life Sciences54171
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code2 codes
  • Services-Commercial Physical & Biological Research8731
  • Services-Medical Laboratories8071
Product category
Preclinical Contract Research Organization (CRO) Services
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Fee-for-Service (FFS) and FTE Models
TypeProfessional Services
Description

Medicilon provides preclinical CRO services using fee-for-service (FFS) and full-time equivalent (FTE) models. The FFS model is used for specific compound synthesis and studies, while FTE models provide dedicated chemist resources for ongoing projects. Services span drug discovery, CMC development, and preclinical research with pricing based on study type, duration, and resource allocation.

medicilon.com
Marketing channels4 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, Technology or R&D, Infrastructure, Marketing or Sales
Pricing details1 tier
1Custom project-based pricing
ModelOtherBilling cadenceMulti-year contract
Notes

Quote-based / Not publicly disclosed - Services are tailored to client project requirements with pricing based on study type, compounds, timelines, and resource needs.

medicilon.com
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

Shanghai Medicilon is a preclinical contract research organization (CRO) that provides integrated drug discovery, CMC (chemistry, manufacturing and controls) development, and IND-enabling preclinical research services to pharmaceutical and biotechnology companies. Its offering spans discovery chemistry and biology, process development and formulation, and safety assessment / regulatory support, backed by advanced technology platforms for peptides, siRNA, ADCs, PROTACs, AOCs, and NAMs toxicology.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • 580+ IND-approved projects delivered
+5 more records
Product overview1 text field

Medicilon is an integrated preclinical CRO offering unified drug development services spanning drug discovery (chemistry and biology), CMC development, and preclinical research. The portfolio includes core service lines (Drug Discovery Services, CMC Development, Preclinical Research Services) supplemented by six advanced technology platforms: Peptide Drug Discovery Platform (mRNA display), siRNA Platform, ADC Platform, PROTAC Platform, AOC Biology Platform, and NAMs Platform. The company operates from Shanghai with facilities in the US (Boston Innovation Center), supporting 580+ IND-approved projects with over 20 years of experience serving global pharmaceutical and biotech clients.

Product and service1 record
1Drug Discovery Services
CategoryPreclinical CRO — Drug Discovery
Scale indicator15 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-05-01
Description

Medicilon supports Oncotelic Therapeutics' Sapu003 (Deciparticle formulation of everolimus) Phase 1b trial for advanced mTOR-sensitive solid tumors. The joint venture GMP Biotechnology Limited is advancing multiple Deciparticle nanoparticle candidates including OT-101/IL-2 combination therapy. Medicilon's CMC and preclinical capabilities support the JV pipeline including formalization of GMP Bio subsidiaries (Sapu Bio and Sapu Nano).

Strategic tierMinorTypeOthersAnnounced on2024-08-01
Description

Otsuka Pharmaceutical acquired US-based Jnana Therapeutics Inc. in August 2024, gaining access to the oral therapy candidate JNT-517 for phenylketonuria and additional autoimmune pipeline programs. This represents an acquisition rather than a partnership with Medicilon.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2023-07-01
Description

AbbVie extended its partnership with Calibr (a division of Scripps Research) in July 2023 to jointly advance preclinical and early clinical assets, building on an existing relationship. This represents a third-party partnership referenced in market news rather than a direct Medicilon partnership.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

China-based, full-service preclinical and clinical CRO/CDMO with global footprint. Directly comparable integrated discovery-to-IND platform, though materially larger and broader in scope than Medicilon.

TypeDirect peer
Description

China-headquartered preclinical CRO/CDMO offering drug discovery, CMC, DMPK, and safety assessment. Closest head-to-head competitor to Medicilon in the integrated preclinical CRO space.

TypeDirect peer
Description

Global leader in preclinical CRO services including safety assessment, DMPK, and research models. Directly comparable on the preclinical and safety-assessment side of Medicilon's portfolio.

TypeDirect peer
Description

Major global CRO offering preclinical through clinical services with strong DMPK, safety, and CMC capabilities. Comparable end-to-end preclinical offering for large pharma and biotech clients.

TypeRegional player
Description

China-headquartered clinical CRO with growing preclinical/biomarker capabilities. More clinical-stage focused than Medicilon but competes for the same Chinese biotech R&D budgets.

TypeDirect peer
Description

China-based API CDMO with preclinical chemistry and CMC capabilities. Comparable on the small-molecule CMC and process development side of Medicilon's service portfolio.

TypeDirect peer
Description

US- and China-based CRO offering preclinical DMPK, safety, CMC, and bioanalytical services. Comparable integrated preclinical offering with similar US-China dual presence.

TypeBroad incumbent
Description

Global biologics CDMO/CRO offering antibody discovery, cell line development, and biologics manufacturing. Overlaps with Medicilon's antibody/ADC discovery capabilities.

TypeBroad incumbent
Description

Global CRO providing drug discovery, pharmacology, and safety services across multiple modalities. Broader scope but competes for outsourced discovery and preclinical budgets.

TypeBroad incumbent
Description

World's largest CRO with preclinical through clinical capabilities. While primarily clinical-stage, IQVIA's preclinical services compete with Medicilon for large enterprise pharma contracts.

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 highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers4 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 profile1 record

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

Feature9 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles2 records

Each record includes

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

No data
Compliance9 records

Each record includes

Name, Class, Description

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 →

Shanghai Medicilon

Preclinical Contract Research Organization (CRO) Servicesmedicilon.com

Shanghai Medicilon firmographics

Firmographics
Name
Shanghai Medicilon
Legal name
Medicilon
Website
https://medicilon.com
Company type
Private
Founded year
2004
Operating status
Operating
Headcount range
1,001–5,000 employees
Ownership category
akta.pro rank

Shanghai Medicilon industry classification

Industry
Product category
Preclinical Contract Research Organization (CRO) Services
NAICS
Scientific Research and Development Services (5417), Research and Development in the Physical, Engineering, and Life Sciences (54171), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Services-Commercial Physical & Biological Research (8731), Services-Medical Laboratories (8071)
akta.pro primary industry
Preclinical CROs (Discovery/Pharmacology/DMPK) (HLAGAAAB)
akta.pro secondary industries
Toxicology & Safety Assessment CROs (GLP) (HLAGAAAC), Regulatory Strategy & Global Submissions (IND/CTA/NDA/BLA/MAA) (HLAGAKAA), Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC) (HLAGAHAM)

Keywords

  • Preclinical CRO services
  • Drug discovery services
  • CMC development
  • IND-enabling studies
  • Safety assessment services

Where Shanghai Medicilon is headquartered

Location

Headquarters

HQ city
Shanghai
HQ country
China
HQ region
Asia

Offices3 records

Markets served

Shanghai Medicilon business model

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

Revenue model

  1. Fee-for-Service (FFS) and FTE Models: Medicilon provides preclinical CRO services using fee-for-service (FFS) and full-time equivalent (FTE) models. The FFS model is used for specific compound synthesis and studies, while FTE models provide dedicated chemist resources for ongoing projects. Services span drug discovery, CMC development, and preclinical research with pricing based on study type, duration, and resource allocation.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractCustom project-based pricing

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

Shanghai Medicilon product offering

Product offering

Core offering

Shanghai Medicilon is a preclinical contract research organization (CRO) that provides integrated drug discovery, CMC (chemistry, manufacturing and controls) development, and IND-enabling preclinical research services to pharmaceutical and biotechnology companies. Its offering spans discovery chemistry and biology, process development and formulation, and safety assessment / regulatory support, backed by advanced technology platforms for peptides, siRNA, ADCs, PROTACs, AOCs, and NAMs toxicology.

Product overview

Medicilon is an integrated preclinical CRO offering unified drug development services spanning drug discovery (chemistry and biology), CMC development, and preclinical research. The portfolio includes core service lines (Drug Discovery Services, CMC Development, Preclinical Research Services) supplemented by six advanced technology platforms: Peptide Drug Discovery Platform (mRNA display), siRNA Platform, ADC Platform, PROTAC Platform, AOC Biology Platform, and NAMs Platform. The company operates from Shanghai with facilities in the US (Boston Innovation Center), supporting 580+ IND-approved projects with over 20 years of experience serving global pharmaceutical and biotech clients.

Differentiator

Problem solved

Functional benefit

Products and services

  • Drug Discovery Services

Quantifiable outcome

  • 580+ IND-approved projects delivered
  • +5 more outcomes

Companies that use Shanghai Medicilon

Customer profile

Named customers4 records

Segments3 records

Ideal customer profiles1 record

Shanghai Medicilon technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature9 records

Shanghai Medicilon partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered core and minor.

  • Oncotelic TherapeuticscoreStrategic or Co-development Partner · 1 May 2026Medicilon supports Oncotelic Therapeutics' Sapu003 (Deciparticle formulation of everolimus) Phase 1b trial for advanced mTOR-sensitive solid tumors. The joint venture GMP Biotechnology Limited is advancing multiple Deciparticle nanoparticle candidates including OT-101/IL-2 combination therapy. Medicilon's CMC and preclinical capabilities support the JV pipeline including formalization of GMP Bio subsidiaries (Sapu Bio and Sapu Nano).
  • Otsuka PharmaceuticalminorOthers · 1 August 2024Otsuka Pharmaceutical acquired US-based Jnana Therapeutics Inc. in August 2024, gaining access to the oral therapy candidate JNT-517 for phenylketonuria and additional autoimmune pipeline programs. This represents an acquisition rather than a partnership with Medicilon.
  • Calibr (Scripps Research)minorStrategic or Co-development Partner · 1 July 2023AbbVie extended its partnership with Calibr (a division of Scripps Research) in July 2023 to jointly advance preclinical and early clinical assets, building on an existing relationship. This represents a third-party partnership referenced in market news rather than a direct Medicilon partnership.

Scale indicators15 records

Recent moves6 records

Expansion highlights5 records

Shanghai Medicilon competitors and assessment

Company assessment

Direct peers

  • WuXi AppTec: China-based, full-service preclinical and clinical CRO/CDMO with global footprint. Directly comparable integrated discovery-to-IND platform, though materially larger and broader in scope than Medicilon.
  • Pharmaron: China-headquartered preclinical CRO/CDMO offering drug discovery, CMC, DMPK, and safety assessment. Closest head-to-head competitor to Medicilon in the integrated preclinical CRO space.
  • Charles River Laboratories: Global leader in preclinical CRO services including safety assessment, DMPK, and research models. Directly comparable on the preclinical and safety-assessment side of Medicilon's portfolio.
  • Labcorp Drug Development (Covance): Major global CRO offering preclinical through clinical services with strong DMPK, safety, and CMC capabilities. Comparable end-to-end preclinical offering for large pharma and biotech clients.
  • Asymchem Laboratories: China-based API CDMO with preclinical chemistry and CMC capabilities. Comparable on the small-molecule CMC and process development side of Medicilon's service portfolio.
  • Frontage Laboratories: US- and China-based CRO offering preclinical DMPK, safety, CMC, and bioanalytical services. Comparable integrated preclinical offering with similar US-China dual presence.

Regional players

  • Tigermed: China-headquartered clinical CRO with growing preclinical/biomarker capabilities. More clinical-stage focused than Medicilon but competes for the same Chinese biotech R&D budgets.

Broad incumbents

  • WuXi Biologics: Global biologics CDMO/CRO offering antibody discovery, cell line development, and biologics manufacturing. Overlaps with Medicilon's antibody/ADC discovery capabilities.
  • Eurofins Discovery: Global CRO providing drug discovery, pharmacology, and safety services across multiple modalities. Broader scope but competes for outsourced discovery and preclinical budgets.
  • IQVIA: World's largest CRO with preclinical through clinical capabilities. While primarily clinical-stage, IQVIA's preclinical services compete with Medicilon for large enterprise pharma contracts.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

Shanghai Medicilon social profiles

Digital presence

Shanghai Medicilon compliance and trust

Trust signal

Compliance9 records

Shanghai Medicilon financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Shanghai Medicilon leadership team

Management profile

Number of profiles

Profiles2 records

Shanghai Medicilon funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors3 records

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

Shanghai Medicilon 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 Shanghai Medicilon

What does Shanghai Medicilon do?

Shanghai Medicilon is a preclinical contract research organization (CRO) that provides integrated drug discovery, CMC (chemistry, manufacturing and controls) development, and IND-enabling preclinical research services to pharmaceutical and biotechnology companies. Its offering spans discovery chemistry and biology, process development and formulation, and safety assessment / regulatory support, backed by advanced technology platforms for peptides, siRNA, ADCs, PROTACs, AOCs, and NAMs toxicology.

Is Shanghai Medicilon a public or private company?

Shanghai Medicilon is a private company. It is classified as public and is currently operating.

When was Shanghai Medicilon founded?

Shanghai Medicilon was founded in 2004. It employs 1,001 to 5,000 people.

Where is Shanghai Medicilon based?

Shanghai Medicilon is headquartered in Shanghai, China, in the Asia region.

How does Shanghai Medicilon make money?

One revenue line is on record: fee-for-Service (FFS) and FTE Models.

Who are Shanghai Medicilon's main competitors?

Direct peers on record are WuXi AppTec, Pharmaron, Charles River Laboratories, Labcorp Drug Development (Covance), Asymchem Laboratories and Frontage Laboratories. Tigermed is listed as a regional player. Broad incumbents are WuXi Biologics, Eurofins Discovery and IQVIA.

Does Shanghai Medicilon have an API?

No public API is recorded for Shanghai Medicilon.

What industry is Shanghai Medicilon in?

Shanghai Medicilon's product category is Preclinical Contract Research Organization (CRO) Services. Its primary akta.pro industry code is HLAGAAAB, Preclinical CROs (Discovery/Pharmacology/DMPK), with a secondary code of HLAGAAAC, Toxicology & Safety Assessment CROs (GLP). Its NAICS code is 5417 and its SIC code is 8731.

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Live signals
PR NewswireMedicilon besteht FDA-Inspektion und stärkt globale F&E-ExzellenzMedicilon Preclinical Research (Shanghai) LLC successfully passed its first on-site FDA inspection in seven years on May 20, 2025, receiving an official Establishment Inspection Report (EIR) that assessed its organizational structure, staff qualifications, SOPs, facilities, documentation, quality assurance systems, and computer infrastructure. FDA inspectors praised Medicilon for scientific discipline and operational excellence, with officials expecting continued high-quality data submissions. By end of 2024, Medicilon had facilitated 520 Investigational New Drug (IND) approvals across multiple global regulatory bodies including the FDA, China's NMPA, the EU's EMA, Australia's TGA, and South Korea's KFDA.PR NewswireMedicilon passe avec succès l'inspection de la FDA, réaffirmant ainsi son excellence mondiale en matière de R&DMedicilon Preclinical Research (Shanghai) LLC announced on May 20, 2025, that it had successfully passed an FDA on-site inspection, receiving an official Establishment Inspection Report (EIR) that reaffirmed its standing as a trusted leader in preclinical R&D services. This was Medicilon's first FDA on-site inspection in seven years, during which inspectors evaluated organizational structure, staff qualifications, SOPs, facility integrity, documentation processes, experimental operations, quality assurance systems, and computerized infrastructure. By end of 2024, Medicilon had helped 520 new experimental drugs enter clinical trials through approvals from the NMPA, FDA, EMA, TGA, and KFDA, serving more than 2,000 clients worldwide.PR NewswireMedicilon Passes FDA Inspection, Reinforcing Global R&D ExcellenceMedicilon Preclinical Research (Shanghai) LLC successfully passed an FDA on-site inspection on May 20, 2025, receiving an official Establishment Inspection Report (EIR) that validates its organizational structure, quality assurance systems, facilities, and documentation processes. The FDA inspectors praised Medicilon for its scientific discipline and operational excellence, marking the company's first on-site FDA inspection in seven years and significantly enhancing its regulatory credibility. By the end of 2024, Medicilon had helped 520 INDs enter clinical trials through approvals by regulatory bodies including the FDA, China's NMPA, EU EMA, Australian TGA, and South Korea's KFDA.PR NewswireКомпания Medicilon назначила техническим директором доктора Лилли СюйКомпания Medicilon, контрактная организация доклинических исследований, назначила доктора Лилли Сюй новым техническим директором. Доктор Сюй обладает более чем 30-летним опытом доклинической разработки препаратов и будет руководить технологическими инновациями и глобальным расширением компании. Ранее она занимала руководящие должности в крупных фармацевтических и биотехнологических компаниях, включая Pharmaron, Sanofi и Amgen.PR NewswireMedicilon ernennt Dr. Lilly Xu zur technischen LeiterinMedicilon, a leading preclinical contract research organization (CRO), has appointed Dr. Lilly Xu as its new Chief Technology Officer. Dr. Xu brings over 30 years of preclinical drug development experience, having previously held leadership positions at Pharmaron, Icagen, Purdue Pharma, Sanofi, and Amgen. The appointment is intended to drive technological innovation and strengthen Medicilon's global expansion, supporting its advanced research platforms across nucleic acids, ADCs, PROTACs, antibodies, and cell and gene therapies.PR NewswireSpolečnost Medicilon jmenuje Dr. Lilly Xuovou do funkce technologické ředitelkyMedicilon, a leading contract research organization (CRO) for preclinical research, appointed Dr. Lilly Xu as its new Chief Technology Officer. Dr. Xu brings over 30 years of experience in preclinical drug development, having previously held leadership roles at companies including Pharmaron, Icagen, Purdue Pharma, Sanofi, and Amgen. She will lead technology innovation and global expansion initiatives, supporting the company's platforms in nucleic acids, ADC, PROTAC, antibodies, and cell and gene therapies.PR NewswireMedicilon menuje za svoju hlavnú technologickú riaditeľku Dr. Lilly XuMedicilon, a leading preclinical contract research organization (CRO), appointed Dr. Lilly Xu as its new Chief Technology Officer (CTO). Dr. Xu brings over 30 years of experience in preclinical drug development, having held senior positions at major pharmaceutical and biotechnology companies including Pharmaron, Icagen, Purdue Pharma, Sanofi, and Amgen. She will lead technological innovation and global expansion efforts to strengthen Medicilon's position in preclinical drug development services.PR NewswireMedicilon расширяет глобальное присутствие, открывая второй центр НИОКР в МассачусетсеIn August 2024, Medicilon USA Corp officially began operations at its second research and development center in Lexington, Massachusetts, USA, focused on animal models for PK/PD and toxicology studies. The new facility offers advanced research services including efficacy evaluation of low-molecular drugs and biopharmaceuticals, utilizing over 410 tumor model evaluation models and more than 240 non-tumor animal models. This expansion reflects Medicilon's strategy to deepen collaboration with the global pharmaceutical innovation ecosystem and expand its international service capabilities.PR NewswireSpolečnost Medicilon rozšiřuje svou globální přítomnost a oficiálně v Massachusetts otevírá své druhé výzkumné a vývojové centrumMedicilon USA Corp officially opened its second research and development center in Lexington, Massachusetts, in August 2024. The new facility focuses on animal models for PK/PD and toxicological studies to support accelerated drug development. This expansion aims to strengthen collaboration with industry partners and enhance Medicilon's global preclinical service capabilities.PR NewswireMedicilon rozširuje globálnu pôsobnosť a oficiálne otvára v Massachusetts druhé centrum výskumu a vývojaMedicilon USA Corp officially opened its second research and development center in Lexington, Massachusetts, focusing on animal models for PK/PD and toxicology studies. This expansion aims to enhance global operational capacity and collaboration with US biotechnology partners by leveraging local expertise and advanced laboratory facilities.