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Edara Research Foundation

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uuid002eqae

Namestring
Edara Research Foundation
Legal namestring
Edara Research Foundation
Company typeenum
Private
Founded yearint
2016
Descriptiontext

Edara Research Foundation (ERF) is a privately held, GLP-certified preclinical contract research organization (CRO) headquartered in Hyderabad, India, operating from a ~20,000-25,000 sq. ft. AAALAC-compliant facility. Founded in 2015-2016, ERF offers an integrated portfolio of in-vitro and in-vivo preclinical services spanning general toxicology, genotoxicity testing, analytical chemistry, medical device biocompatibility, agrochemical testing, alternatives to animal testing, histopathology, clinical pathology, pharmacology models, bioassays, and microbiology — supported by specialized infrastructure including a Class 100,000 double-barrier vivarium, nose-only inhalation exposure systems supplied by CH Technologies USA, and dedicated AHU design to prevent cross-contamination.

The company serves enterprise sponsors across pharmaceutical, biotechnology, agrochemical, specialty chemical, and medical device industries, with studies conducted under OECD GLP, USFDA GLP, ISO, and AAALAC frameworks enabling data acceptance for global regulatory submissions including USFDA, EPA, CIBRC, and SENASA (Argentina). The revenue model is professional-services / fee-for-service, with project-based contracts covering study design, conduct, evaluation, and reporting; pricing is quote-based and project-specific with no publicly disclosed rate card. GTM is direct enterprise field sales, with the facility open to sponsor on-site engagement during studies.

ERF's competitive positioning rests on its dense regulatory accreditation stack (NGCMA GLP through 2026, AAALAC, CPCSEA, ISO 9001:2015, ISO/IEC 17025:2017, Telangana Drug Control, DTL, SENASA), India-based cost structure with international data acceptance, and specialized inhalation toxicology and 3Rs-aligned alternative testing capabilities. The company is founder/management-led with no disclosed institutional ownership, no funding rounds, and no M&A activity in the source data.

Short descriptiontext

Edara Research Foundation is a GLP-certified preclinical contract research organization based in Hyderabad, India, providing in-vitro and in-vivo toxicology, genotoxicity, analytical, medical device, and agrochemical testing services to pharmaceutical, biotechnology, and specialty chemical sponsors.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersHyderabad, India
HQ citystring
Hyderabad
HQ countrystring
India
HQ regionstring
Asia
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
preclinical contract research, GLP toxicology services, in-vivo safety studies, regulatory toxicology testing, biocompatibility testing
Industry4 codes
1Toxicology & Safety Assessment CROs (GLP)
CodeHLAGAAACPrimaryYes
2Nonclinical Study Management & Regulatory Writing (IND-enabling)
CodeHLAGAFANPrimaryNo
3Laboratory Quality & GLP/GCLP Compliance
CodeHLAGAKAKPrimaryNo
4Method Development & Validation (ICH/USP)
CodeHLAGADABPrimaryNo
NAICS code2 codes
  • Scientific Research and Development Services5417
  • Research and Development in the Physical, Engineering, and Life Sciences54171
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Preclinical Contract Research Services
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Preclinical Contract Research Services
TypeProfessional Services
Description

Fee-for-service contract research providing GLP-compliant toxicology, pharmacology, DMPK, biocompatibility and pharmacopoeia testing to pharmaceutical, biotech, agrochemical and specialty chemical clients. Revenue generated through project-based contracts with study design, conduct, evaluation and reporting services.

edararesearch.com
Marketing channels2 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, Operations, Technology or R&D, Others, Marketing or Sales
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

Edara Research Foundation provides GLP-compliant preclinical contract research services, executing in-vitro and in-vivo toxicology, genotoxicity, analytical chemistry, pharmacology, histopathology, clinical pathology, bioassays, microbiology, biocompatibility, and agrochemical safety studies under international regulatory guidelines (OECD, ICH, USFDA, EPA, ISO 10993). Services are delivered from a 20,000–25,000 sq. ft. AAALAC-accredited facility in Hyderabad, with an independent QA unit, dedicated project management, and rapid turnaround of regulatory-grade study reports.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • Cost-effective GLP data with rapid turnaround times
Product overview1 text field

Edara Research Foundation (ERF) is a preclinical contract research organization (CRO) offering integrated GLP-compliant research services for the pharmaceutical, biotech, agrochemical, and specialty chemical industries. The company provides a comprehensive portfolio of testing services organized around General Toxicology (core offering), Genotoxicity Testing, Analytical Services, Medical Device Testing (biocompatibility), Agro Chemical Testing, Alternatives to Animal Testing, Histopathology, Clinical Pathology, Pharmacology Models, Bioassays, and Microbiology. These services are supported by state-of-the-art facilities including Animal (vivarium), Inhalation, Clinical Pathology, Histopathology, Analytical Chemistry, and Archives, all designed to deliver seamless preclinical safety and efficacy investigations in compliance with OECD GLP, ISO, AAALAC, and USFDA GLP guidelines.

Product and service11 records
1General Toxicology
CategoryPreclinical Toxicology Services
Description

GLP-compliant toxicology studies per OECD, ICH, Schedule Y, and EPA guidelines, including Maximum Tolerable Dose, Dose Range Finding, Single and Repeated Dose Toxicity, and Skin Sensitization Studies, for pharmaceutical and chemical sponsors.

2Genotoxicity Testing
CategoryPreclinical Toxicology Services
Description

In vitro and in vivo genetic toxicology studies including Bacterial Reverse Mutation Test (Ames test), Micronucleus Tests, and Chromosome Aberration Tests, conducted in compliance with OECD and US-EPA guidelines for regulatory submissions.

3Analytical Services
CategoryAnalytical Chemistry Services
Description

Analytical chemistry services including Five Batch Analysis, Method Development & Validation, Dose Formulation Analysis, Shelf Life Studies, Residue Studies, and Physico-Chemical Testing, performed per OECD/ICH/USP/BP/EP/IP/JP guidelines.

4Medical Device Testing
CategoryMedical Device Biocompatibility Testing
Description

Biocompatibility testing services for medical devices per ISO 10993 and USP standards, covering Cytotoxicity, Skin Sensitization, Eye Irritation, Acute Systemic Toxicity, Implantation, Hemolysis, and Pyrogenicity tests.

5Agro Chemical Testing
CategoryRegulatory Toxicology Services (Agrochemical)
Description

Comprehensive agrochemical testing services including Acute 6-pack studies, Repeated Dose Toxicity, and Genotoxicity studies per CIBRC, OECD, EPA OCSPP, and other regulatory guidelines for crop protection and chemical registration.

6Alternatives to Animal Testing
CategoryAlternative Testing Services
Description

Alternative testing models aligned with 3Rs principle, including Local Lymph Node Assay (LLNA) using BrdU-ELISA, In vitro Skin and Ocular Irritation Studies, and In vitro Dermal Percutaneous Absorption Studies.

7Histopathology
CategoryPreclinical Pathology Services
Description

Histopathology services including Tissue Processing, Embedding, Sectioning, Slide Preparation, and Slide Evaluation to support preclinical toxicology studies.

8Clinical Pathology
CategoryPreclinical Pathology Services
Description

Clinical pathology services including Hematological Parameters, Clinical Chemistry Parameters, Urine Analysis, and ELISA Testing Services for preclinical study support.

9Pharmacology Models
CategoryPharmacology Services
Description

In vivo pharmacology efficacy studies including Pain and Inflammatory Models, Neuropathic Pain Models, and Metabolic Disorder Models to support proof-of-concept advancement of NCEs.

10Bioassays
CategoryBioassay and Pharmacopeial Testing Services
Description

Bioassay testing services per Indian, US, European, and British Pharmacopeia, including Heparin Studies, Anti Factor Xa & IIa Activity, Abnormal Toxicity, Rabbit Pyrogen, Estrogenic Activity, and Endotoxin testing.

11Microbiology
CategoryMicrobiology Testing Services
Description

Microbiology services including Preservative Efficacy Testing, Disinfectant Efficacy Testing, Antibiotic Potency Assay, Endotoxin Testing, Bioburden Testing, and Water Testing.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierCoreTypeTechnology or Integration
Description

CH Technologies USA provides specialized nose-only inhalation exposure systems used for inhalation toxicology testing at ERF. The equipment enables precise control of exposure for each individual animal with concentration adjustment capability in the exposure chamber, attached to dedicated AHU for cross-contamination prevention.

2National GLP Compliance Monitoring Authority (NGCMA)
Strategic tierCoreTypeOthers
Description

Regulatory body that certifies GLP compliance for preclinical research organizations in India. ERF holds GLP compliance certification from NGCMA for conducting regulatory toxicology studies.

edararesearch.com
Strategic tierCoreTypeOthers
Description

Association for Assessment and Accreditation of Laboratory Animal Care International provides voluntary accreditation for animal care and use programs. ERF maintains AAALAC accreditation demonstrating commitment to ethical animal welfare standards.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Hyderabad-based contract testing and research laboratory offering preclinical, analytical, and bioanalytical services to pharma, agrochemical, and food customers. Most comparable Indian direct peer given overlapping GLP toxicology, analytical, and medical-device testing services from the same city.

TypeBroad incumbent
Description

India-based CRO offering integrated drug discovery, development, and CDMO services through Jubilant Pharma. Larger, broader incumbent Indian CRO that overlaps with ERF on preclinical toxicology but operates across a wider portfolio.

TypeBroad incumbent
Description

China-headquartered global CRO/CDMO providing preclinical toxicology, chemistry, and biologics services. As sponsors diversify away from China concentration toward India, ERF is positioned as an alternative to WuXi for outsourced preclinical work.

TypeBroad incumbent
Description

Global testing services provider with significant pharma/agrochemical laboratory and preclinical testing operations across Europe and Asia. Broad incumbent in analytical and safety testing serving overlapping sponsor segments.

TypeDirect peer
Description

Bangalore-based contract research organization providing drug discovery, development, and preclinical services including toxicology studies. Comparable Indian preclinical CRO serving similar global sponsor base.

TypeDirect peer
Description

India-headquartered CRO providing discovery, CMC, and preclinical research services to global pharma and biotech sponsors. Comparable as an Indian-based preclinical CRO competing for international GLP toxicology contracts.

TypeBroad incumbent
Description

Publicly listed Indian CRO/CDMO offering discovery, development, and manufacturing services including preclinical toxicology for global pharma. Larger Indian incumbent with broader service portfolio and stronger brand visibility than ERF.

TypeDirect peer
Description

Indian CRO offering discovery, preclinical, and clinical research services with GLP toxicology capabilities for pharma and agrochemical sponsors. Closely comparable preclinical CRO with overlapping GLP toxicology and chemistry service lines.

TypeBroad incumbent
Description

Global Tier-1 preclinical CRO and safety assessment specialist with extensive GLP toxicology, inhalation, and analytical service lines. The dominant global incumbent ERF competes against for overflow toxicology work from large sponsors.

TypeDirect peer
Description

India-based CRO offering bioanalytical, clinical, and preclinical research services. Comparable Indian CRO with adjacent preclinical/bioanalytical offering to global pharma sponsors.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 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 customers3 records

Each record includes

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

Segment4 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

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
No data
Compliance9 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

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

Investors

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 →

Edara Research Foundation

Preclinical Contract Research Servicesedararesearch.com

Edara Research Foundation is a GLP-certified preclinical contract research organization based in Hyderabad, India, providing in-vitro and in-vivo toxicology, genotoxicity, analytical, medical device, and agrochemical testing services to pharmaceutical, biotechnology, and specialty chemical sponsors.

What Edara Research Foundation does

Edara Research Foundation (ERF) is a privately held, GLP-certified preclinical contract research organization (CRO) headquartered in Hyderabad, India, operating from a ~20,000-25,000 sq. ft. AAALAC-compliant facility. Founded in 2015-2016, ERF offers an integrated portfolio of in-vitro and in-vivo preclinical services spanning general toxicology, genotoxicity testing, analytical chemistry, medical device biocompatibility, agrochemical testing, alternatives to animal testing, histopathology, clinical pathology, pharmacology models, bioassays, and microbiology — supported by specialized infrastructure including a Class 100,000 double-barrier vivarium, nose-only inhalation exposure systems supplied by CH Technologies USA, and dedicated AHU design to prevent cross-contamination.

The company serves enterprise sponsors across pharmaceutical, biotechnology, agrochemical, specialty chemical, and medical device industries, with studies conducted under OECD GLP, USFDA GLP, ISO, and AAALAC frameworks enabling data acceptance for global regulatory submissions including USFDA, EPA, CIBRC, and SENASA (Argentina). The revenue model is professional-services / fee-for-service, with project-based contracts covering study design, conduct, evaluation, and reporting; pricing is quote-based and project-specific with no publicly disclosed rate card. GTM is direct enterprise field sales, with the facility open to sponsor on-site engagement during studies.

ERF's competitive positioning rests on its dense regulatory accreditation stack (NGCMA GLP through 2026, AAALAC, CPCSEA, ISO 9001:2015, ISO/IEC 17025:2017, Telangana Drug Control, DTL, SENASA), India-based cost structure with international data acceptance, and specialized inhalation toxicology and 3Rs-aligned alternative testing capabilities. The company is founder/management-led with no disclosed institutional ownership, no funding rounds, and no M&A activity in the source data.

Edara Research Foundation firmographics

Firmographics
Name
Edara Research Foundation
Legal name
Edara Research Foundation
Website
https://edararesearch.com
Company type
Private
Founded year
2016
Operating status
Operating
Headcount range
51–100 employees
Short description
Edara Research Foundation is a GLP-certified preclinical contract research organization based in Hyderabad, India, providing in-vitro and in-vivo toxicology, genotoxicity, analytical, medical device, and agrochemical testing services to pharmaceutical, biotechnology, and specialty chemical sponsors.
Ownership category
akta.pro rank

Edara Research Foundation industry classification

Industry
Product category
Preclinical Contract Research Services
NAICS
Scientific Research and Development Services (5417), Research and Development in the Physical, Engineering, and Life Sciences (54171)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Toxicology & Safety Assessment CROs (GLP) (HLAGAAAC)
akta.pro secondary industries
Nonclinical Study Management & Regulatory Writing (IND-enabling) (HLAGAFAN), Laboratory Quality & GLP/GCLP Compliance (HLAGAKAK), Method Development & Validation (ICH/USP) (HLAGADAB)

Keywords

  • Preclinical contract research
  • GLP toxicology services
  • In-vivo safety studies
  • Regulatory toxicology testing
  • Biocompatibility testing

Where Edara Research Foundation is headquartered

Location

Headquarters

HQ city
Hyderabad
HQ country
India
HQ region
Asia

Offices1 record

Markets served

Edara Research Foundation business model

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

Revenue model

  1. Preclinical Contract Research Services: Fee-for-service contract research providing GLP-compliant toxicology, pharmacology, DMPK, biocompatibility and pharmacopoeia testing to pharmaceutical, biotech, agrochemical and specialty chemical clients. Revenue generated through project-based contracts with study design, conduct, evaluation and reporting services.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels2 records

Edara Research Foundation product offering

Product offering

Core offering

Edara Research Foundation provides GLP-compliant preclinical contract research services, executing in-vitro and in-vivo toxicology, genotoxicity, analytical chemistry, pharmacology, histopathology, clinical pathology, bioassays, microbiology, biocompatibility, and agrochemical safety studies under international regulatory guidelines (OECD, ICH, USFDA, EPA, ISO 10993). Services are delivered from a 20,000–25,000 sq. ft. AAALAC-accredited facility in Hyderabad, with an independent QA unit, dedicated project management, and rapid turnaround of regulatory-grade study reports.

Product overview

Edara Research Foundation (ERF) is a preclinical contract research organization (CRO) offering integrated GLP-compliant research services for the pharmaceutical, biotech, agrochemical, and specialty chemical industries. The company provides a comprehensive portfolio of testing services organized around General Toxicology (core offering), Genotoxicity Testing, Analytical Services, Medical Device Testing (biocompatibility), Agro Chemical Testing, Alternatives to Animal Testing, Histopathology, Clinical Pathology, Pharmacology Models, Bioassays, and Microbiology. These services are supported by state-of-the-art facilities including Animal (vivarium), Inhalation, Clinical Pathology, Histopathology, Analytical Chemistry, and Archives, all designed to deliver seamless preclinical safety and efficacy investigations in compliance with OECD GLP, ISO, AAALAC, and USFDA GLP guidelines.

Differentiator

Problem solved

Functional benefit

Products and services

  • General Toxicology GLP-compliant toxicology studies per OECD, ICH, Schedule Y, and EPA guidelines, including Maximum Tolerable Dose, Dose Range Finding, Single and Repeated Dose Toxicity, and Skin Sensitization Studies, for pharmaceutical and chemical sponsors.
  • Genotoxicity Testing In vitro and in vivo genetic toxicology studies including Bacterial Reverse Mutation Test (Ames test), Micronucleus Tests, and Chromosome Aberration Tests, conducted in compliance with OECD and US-EPA guidelines for regulatory submissions.
  • Analytical Services Analytical chemistry services including Five Batch Analysis, Method Development & Validation, Dose Formulation Analysis, Shelf Life Studies, Residue Studies, and Physico-Chemical Testing, performed per OECD/ICH/USP/BP/EP/IP/JP guidelines.
  • Medical Device Testing Biocompatibility testing services for medical devices per ISO 10993 and USP standards, covering Cytotoxicity, Skin Sensitization, Eye Irritation, Acute Systemic Toxicity, Implantation, Hemolysis, and Pyrogenicity tests.
  • Agro Chemical Testing Comprehensive agrochemical testing services including Acute 6-pack studies, Repeated Dose Toxicity, and Genotoxicity studies per CIBRC, OECD, EPA OCSPP, and other regulatory guidelines for crop protection and chemical registration.
  • Alternatives to Animal Testing Alternative testing models aligned with 3Rs principle, including Local Lymph Node Assay (LLNA) using BrdU-ELISA, In vitro Skin and Ocular Irritation Studies, and In vitro Dermal Percutaneous Absorption Studies.
  • Histopathology Histopathology services including Tissue Processing, Embedding, Sectioning, Slide Preparation, and Slide Evaluation to support preclinical toxicology studies.
  • Clinical Pathology Clinical pathology services including Hematological Parameters, Clinical Chemistry Parameters, Urine Analysis, and ELISA Testing Services for preclinical study support.
  • Pharmacology Models In vivo pharmacology efficacy studies including Pain and Inflammatory Models, Neuropathic Pain Models, and Metabolic Disorder Models to support proof-of-concept advancement of NCEs.
  • Bioassays Bioassay testing services per Indian, US, European, and British Pharmacopeia, including Heparin Studies, Anti Factor Xa & IIa Activity, Abnormal Toxicity, Rabbit Pyrogen, Estrogenic Activity, and Endotoxin testing.
  • Microbiology Microbiology services including Preservative Efficacy Testing, Disinfectant Efficacy Testing, Antibiotic Potency Assay, Endotoxin Testing, Bioburden Testing, and Water Testing.

Quantifiable outcome

  • Cost-effective GLP data with rapid turnaround times

Companies that use Edara Research Foundation

Customer profile

Named customers3 records

Segments4 records

Ideal customer profiles3 records

Edara Research Foundation technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Edara Research Foundation partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered core.

  • CH Technologies USAcoreTechnology or IntegrationCH Technologies USA provides specialized nose-only inhalation exposure systems used for inhalation toxicology testing at ERF. The equipment enables precise control of exposure for each individual animal with concentration adjustment capability in the exposure chamber, attached to dedicated AHU for cross-contamination prevention.
  • National GLP Compliance Monitoring Authority (NGCMA)coreOthersRegulatory body that certifies GLP compliance for preclinical research organizations in India. ERF holds GLP compliance certification from NGCMA for conducting regulatory toxicology studies.
  • AAALAC InternationalcoreOthersAssociation for Assessment and Accreditation of Laboratory Animal Care International provides voluntary accreditation for animal care and use programs. ERF maintains AAALAC accreditation demonstrating commitment to ethical animal welfare standards.

Scale indicators3 records

Recent moves6 records

Expansion highlights5 records

Edara Research Foundation competitors and assessment

Company assessment

Direct peers

  • Vimta Labs: Hyderabad-based contract testing and research laboratory offering preclinical, analytical, and bioanalytical services to pharma, agrochemical, and food customers. Most comparable Indian direct peer given overlapping GLP toxicology, analytical, and medical-device testing services from the same city.
  • Anthem Biosciences: Bangalore-based contract research organization providing drug discovery, development, and preclinical services including toxicology studies. Comparable Indian preclinical CRO serving similar global sponsor base.
  • Sai Life Sciences: India-headquartered CRO providing discovery, CMC, and preclinical research services to global pharma and biotech sponsors. Comparable as an Indian-based preclinical CRO competing for international GLP toxicology contracts.
  • Aragen (formerly GVK Biosciences): Indian CRO offering discovery, preclinical, and clinical research services with GLP toxicology capabilities for pharma and agrochemical sponsors. Closely comparable preclinical CRO with overlapping GLP toxicology and chemistry service lines.
  • Veeda Lifesciences (Veeda Clinical Research): India-based CRO offering bioanalytical, clinical, and preclinical research services. Comparable Indian CRO with adjacent preclinical/bioanalytical offering to global pharma sponsors.

Broad incumbents

  • Jubilant Biosys: India-based CRO offering integrated drug discovery, development, and CDMO services through Jubilant Pharma. Larger, broader incumbent Indian CRO that overlaps with ERF on preclinical toxicology but operates across a wider portfolio.
  • WuXi AppTec: China-headquartered global CRO/CDMO providing preclinical toxicology, chemistry, and biologics services. As sponsors diversify away from China concentration toward India, ERF is positioned as an alternative to WuXi for outsourced preclinical work.
  • Eurofins Scientific: Global testing services provider with significant pharma/agrochemical laboratory and preclinical testing operations across Europe and Asia. Broad incumbent in analytical and safety testing serving overlapping sponsor segments.
  • Syngene International: Publicly listed Indian CRO/CDMO offering discovery, development, and manufacturing services including preclinical toxicology for global pharma. Larger Indian incumbent with broader service portfolio and stronger brand visibility than ERF.
  • Charles River Laboratories: Global Tier-1 preclinical CRO and safety assessment specialist with extensive GLP toxicology, inhalation, and analytical service lines. The dominant global incumbent ERF competes against for overflow toxicology work from large sponsors.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Edara Research Foundation social profiles

Digital presence

Edara Research Foundation compliance and trust

Trust signal

Compliance9 records

Edara Research Foundation financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Edara Research Foundation leadership team

Management profile

Number of profiles

Edara Research Foundation funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Edara Research Foundation 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 Edara Research Foundation

What does Edara Research Foundation do?

Edara Research Foundation provides GLP-compliant preclinical contract research services, executing in-vitro and in-vivo toxicology, genotoxicity, analytical chemistry, pharmacology, histopathology, clinical pathology, bioassays, microbiology, biocompatibility, and agrochemical safety studies under international regulatory guidelines (OECD, ICH, USFDA, EPA, ISO 10993). Services are delivered from a 20,000–25,000 sq. ft. AAALAC-accredited facility in Hyderabad, with an independent QA unit, dedicated project management, and rapid turnaround of regulatory-grade study reports.

Is Edara Research Foundation a public or private company?

Edara Research Foundation is a private company. It is classified as unknown and is currently operating.

When was Edara Research Foundation founded?

Edara Research Foundation was founded in 2016. It employs 51 to 100 people.

Where is Edara Research Foundation based?

Edara Research Foundation is headquartered in Hyderabad, India, in the Asia region.

How does Edara Research Foundation make money?

One revenue line is on record: preclinical Contract Research Services.

Who are Edara Research Foundation's main competitors?

Direct peers on record are Vimta Labs, Anthem Biosciences, Sai Life Sciences, Aragen (formerly GVK Biosciences) and Veeda Lifesciences (Veeda Clinical Research). Broad incumbents are Jubilant Biosys, WuXi AppTec, Eurofins Scientific, Syngene International and Charles River Laboratories.

Does Edara Research Foundation have an API?

No public API is recorded for Edara Research Foundation.

What industry is Edara Research Foundation in?

Edara Research Foundation's product category is Preclinical Contract Research Services. Its primary akta.pro industry code is HLAGAAAC, Toxicology & Safety Assessment CROs (GLP), with a secondary code of HLAGAFAN, Nonclinical Study Management & Regulatory Writing (IND-enabling). Its NAICS code is 5417 and its SIC code is 8731.

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