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ClinSync Clinical Research Pvt Ltd

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uuid0045ju8

Namestring
ClinSync Clinical Research Pvt Ltd
Legal namestring
ClinSync Clinical Research Pvt. Ltd.
Websiteurl
clinsync.com
Company typeenum
Private
Founded yearint
2011
Descriptiontext

ClinSync Clinical Research Pvt. Ltd. is a Hyderabad-based contract research organization (CRO) established in 2011 that delivers end-to-end clinical research services to pharmaceutical, biotech, biosimilar, and medical device sponsors. Its service portfolio spans Bioavailability/Bioequivalence (BA/BE) studies, Phase II-IV clinical trial operations, bioanalytical method development and sample analysis, clinical data management, pharmacokinetics and biostatistics, pharmacovigilance, medical writing, cold-chain sample management, and (since 2022) FMCG/personal healthcare testing. The company reports more than 390 completed BA/BE studies, 14+ clinical trials, and 100+ method validations across its history, with named customers including Hetero, Aurobindo, Sun Pharma, Alembic, MSN Laboratories, Syngene, Mayo Clinic, and OmniActive.

The company's technical platform is anchored by a 160-bed clinical pharmacology unit (with ICU facilities) at Madeenaguda, Hyderabad, and eight LC-MS/MS systems (API 4000 and API 4500) capable of processing over 30,000 samples per month. Bioanalytical work is supported by a method data bank of 100+ validated assays aligned with FDA, EMEA, NPRA, ANVISA, TGA, and DCGI standards, and clinical data management operates across Medidata Rave, Oracle Clinical RDC, Data Labs, and Inform under 21 CFR Part 11 compliant systems. Pharmacokinetic analysis is performed in Phoenix WinNonlin (v8.3) with statistical analysis in SAS (v9.4), supporting parallel, 2-way crossover, 3-way reference replicate, and 4-way full replicate designs. ClinSync has cleared six USFDA inspections, including a 2023 inspection with zero 483 observations, and holds DSIR recognition in addition to CDSCO, GCC, and NPRA accreditations.

ClinSync operates a fee-for-service, project-based B2B model: revenue is generated through customized study contracts, with pricing determined by study type, complexity, therapeutic area, subject count, and regulatory submission target. Go-to-market is direct enterprise sales via a dedicated business development team, supplemented by participation in industry events and inbound inquiries through [email protected]. The company is privately held, founder/management-owned (per available data, with no disclosed institutional backers or funding rounds), employs 130-148 professionals, and is headquartered in Telangana, India, serving clients across South Asia and select global sponsors.

Short descriptiontext

Hyderabad-based ClinSync Clinical Research is a CRO providing BA/BE studies, Phase II-IV clinical trials, bioanalytical services, and clinical data management to pharmaceutical, biotech, biosimilar, and medical device sponsors. Founded 2011, it operates a 160-bed facility staffed by 130+ professionals.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersHyderabad (Madeenaguda), India
HQ citystring
Hyderabad (Madeenaguda)
HQ countrystring
India
HQ regionstring
Asia
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical research services, bioavailability bioequivalence studies, bioanalytical services, clinical data management, contract research organization
Industry3 codes
1Clinical CROs (Phase I–IV)
CodeHLAGAAAAPrimaryYes
2DMPK / ADME & Bioanalysis
CodeHLAGAFACPrimaryNo
3Central Laboratory & Clinical Trial Testing CROs
CodeHLAGAAAEPrimaryNo
NAICS code2 codes
  • Research and Development in the Physical, Engineering, and Life Sciences54171
  • Medical and Diagnostic Laboratories62151
SIC code2 codes
  • Services-Commercial Physical & Biological Research8731
  • Services-Medical Laboratories8071
Product category
Contract Research Organization (CRO) Services
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Clinical Research Services
TypeProfessional Services
Description

Fee-for-service B2B model providing end-to-end clinical research services to pharmaceutical, biotech, biosimilar, and medical device companies. Revenue generated through project-based contracts for BA/BE studies, clinical trials, data management, bioanalytical services, and medical writing.

clinsync.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

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
1Project-based service pricing
ModelOtherBilling cadenceMulti-year contract
Notes

Quote-based / Not publicly disclosed. Customized to client requirements.

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

ClinSync Clinical Research Pvt Ltd is a Contract Research Organization that delivers outsourced clinical research services to pharmaceutical, biotechnology, biosimilar, and medical device companies. The company conducts Bioavailability/Bioequivalence (BA/BE) studies, Phase II-IV clinical trials, clinical data management, and bioanalytical laboratory analyses on a fee-for-service basis.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 7 values shown
  • 390+ BA/BE studies completed
+6 more records
Product overview1 text field

ClinSync Clinical Research Pvt Ltd is a Contract Research Organization (CRO) established in 2011 in India, providing comprehensive end-to-end services to pharmaceutical, biotech, biosimilar, and medical device industries. The company operates as a unified platform offering BA/BE Studies (390+ completed), Clinical Trial Operations (Phase II-IV), Clinical Data Management, Bioanalytical Services, Clinical Pharmacology, Pharmacokinetics/Biostatistics, Medical Writing, Cold Chain Management, and Personal Healthcare (FMCG) testing services. With a 160-bed clinical facility and 130+ professionals, the company integrates these services to support drug development from early-phase bioequivalence studies through late-phase clinical trials and regulatory submissions.

Product and service4 records
1Bioavailability/Bioequivalence (BA/BE) Studies
CategoryClinical Research Services
Description

Conducted for pharmaceutical and biosimilar manufacturers requiring regulatory bioequivalence data for generic drug submissions and comparative pharmacokinetic studies.

2Clinical Trials (Phase II-IV)
CategoryClinical Research Services
Description

Phase II through Phase IV clinical trial design, conduct, and monitoring services for pharmaceutical, biotechnology, and medical device sponsors across multiple therapeutic areas.

3Clinical Data Management
CategoryClinical Data Management Services
Description

Clinical trial database design, data entry, validation, discrepancy management, and database lock services for sponsors running clinical studies.

4Bioanalytical Services
CategoryBioanalytical Laboratory Services
Description

Laboratory bioanalytical method development, validation, and sample analysis for pharmacokinetic, bioavailability, and bioequivalence studies, supporting both clinical trials and standalone bioanalytical projects.

Scale indicator11 records

Each record includes

Type, Value, Description, Source

Recent move9 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

India-based integrated CRO/CDMO serving global pharma and biotech with clinical development, bioanalytical, and data management services. Syngene is a direct peer — also a listed ClinSync customer and competitor for outsourced clinical and bioanalytical work out of India.

TypeBroad incumbent
Description

Global CRO offering Phase I-IV clinical operations, bioanalytical, regulatory, and post-approval services. Parexel is a broad incumbent competitor for multi-country Phase II-IV and bioequivalence work that large pharma sponsors might award instead of a mid-sized Indian CRO.

TypeDirect peer
Description

Indian CRO providing BA/BE, Phase I-IV clinical trials, bioanalytical, and clinical data management services. Lambda is a direct competitor targeting the same generic and biosimilar sponsor base with similar service breadth.

TypeDirect peer
Description

Indian CRO with multi-therapeutic clinical research, bioanalytical, and dermatology/cosmetics testing capabilities. Cliantha competes with ClinSync in both pharma BA/BE and the Personal Healthcare/FMCG testing vertical ClinSync launched in 2022.

TypeBroad incumbent
Description

Global full-service CRO and clinical technology provider. IQVIA is a broad incumbent that competes for the same Phase II-IV clinical trial and bioanalytical work as ClinSync, with substantially larger global footprint, therapeutic breadth, and scale.

TypeDirect peer
Description

Indian CRO headquartered in Ahmedabad offering BA/BE studies, bioanalytical services, and clinical research across therapeutic areas. Veeda is one of ClinSync's closest head-to-head competitors for Indian generic sponsor BA/BE and Phase II-IV outsourcing.

TypeDirect peer
Description

Hyderabad-headquartered CRO/CDMO offering clinical research, bioanalytical, and discovery services to global pharma. GVK BIO is a directly comparable Indian CRO competing for the same Hyderabad-based sponsor relationships and talent pool.

TypeRegional player
Description

China-headquartered CRO/CDMO offering laboratory, bioanalytical, and clinical research services across geographies. Pharmaron is a regional peer — operates in the same Asia-based outsourcing value proposition that Indian CROs like ClinSync compete within for global sponsor BA/BE and clinical work.

TypeBroad incumbent
Description

Global CRO with extensive bioanalytical, central lab, and early-stage clinical capabilities. Labcorp is a broad incumbent that competes for global pharma BA/BE and Phase II-IV work, including USFDA-submission programs that Indian CROs target.

TypeBroad incumbent
Description

Global CRO providing bioanalytical, safety, and clinical research services. Charles River is a broad incumbent competing for the same regulated bioanalytical and Phase II-IV work, particularly for large pharma and biotech sponsors.

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 customers11 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 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
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
No data
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 →

ClinSync Clinical Research Pvt Ltd

Contract Research Organization (CRO) Servicesclinsync.com

Hyderabad-based ClinSync Clinical Research is a CRO providing BA/BE studies, Phase II-IV clinical trials, bioanalytical services, and clinical data management to pharmaceutical, biotech, biosimilar, and medical device sponsors. Founded 2011, it operates a 160-bed facility staffed by 130+ professionals.

What ClinSync Clinical Research Pvt Ltd does

ClinSync Clinical Research Pvt. Ltd. is a Hyderabad-based contract research organization (CRO) established in 2011 that delivers end-to-end clinical research services to pharmaceutical, biotech, biosimilar, and medical device sponsors. Its service portfolio spans Bioavailability/Bioequivalence (BA/BE) studies, Phase II-IV clinical trial operations, bioanalytical method development and sample analysis, clinical data management, pharmacokinetics and biostatistics, pharmacovigilance, medical writing, cold-chain sample management, and (since 2022) FMCG/personal healthcare testing. The company reports more than 390 completed BA/BE studies, 14+ clinical trials, and 100+ method validations across its history, with named customers including Hetero, Aurobindo, Sun Pharma, Alembic, MSN Laboratories, Syngene, Mayo Clinic, and OmniActive.

The company's technical platform is anchored by a 160-bed clinical pharmacology unit (with ICU facilities) at Madeenaguda, Hyderabad, and eight LC-MS/MS systems (API 4000 and API 4500) capable of processing over 30,000 samples per month. Bioanalytical work is supported by a method data bank of 100+ validated assays aligned with FDA, EMEA, NPRA, ANVISA, TGA, and DCGI standards, and clinical data management operates across Medidata Rave, Oracle Clinical RDC, Data Labs, and Inform under 21 CFR Part 11 compliant systems. Pharmacokinetic analysis is performed in Phoenix WinNonlin (v8.3) with statistical analysis in SAS (v9.4), supporting parallel, 2-way crossover, 3-way reference replicate, and 4-way full replicate designs. ClinSync has cleared six USFDA inspections, including a 2023 inspection with zero 483 observations, and holds DSIR recognition in addition to CDSCO, GCC, and NPRA accreditations.

ClinSync operates a fee-for-service, project-based B2B model: revenue is generated through customized study contracts, with pricing determined by study type, complexity, therapeutic area, subject count, and regulatory submission target. Go-to-market is direct enterprise sales via a dedicated business development team, supplemented by participation in industry events and inbound inquiries through [email protected]. The company is privately held, founder/management-owned (per available data, with no disclosed institutional backers or funding rounds), employs 130-148 professionals, and is headquartered in Telangana, India, serving clients across South Asia and select global sponsors.

ClinSync Clinical Research Pvt Ltd firmographics

Firmographics
Name
ClinSync Clinical Research Pvt Ltd
Legal name
ClinSync Clinical Research Pvt. Ltd.
Website
https://clinsync.com
Company type
Private
Founded year
2011
Operating status
Operating
Headcount range
101–250 employees
Short description
Hyderabad-based ClinSync Clinical Research is a CRO providing BA/BE studies, Phase II-IV clinical trials, bioanalytical services, and clinical data management to pharmaceutical, biotech, biosimilar, and medical device sponsors. Founded 2011, it operates a 160-bed facility staffed by 130+ professionals.
Ownership category
akta.pro rank

ClinSync Clinical Research Pvt Ltd industry classification

Industry
Product category
Contract Research Organization (CRO) Services
NAICS
Research and Development in the Physical, Engineering, and Life Sciences (54171), Medical and Diagnostic Laboratories (62151)
SIC
Services-Commercial Physical & Biological Research (8731), Services-Medical Laboratories (8071)
akta.pro primary industry
Clinical CROs (Phase I–IV) (HLAGAAAA)
akta.pro secondary industries
DMPK / ADME & Bioanalysis (HLAGAFAC), Central Laboratory & Clinical Trial Testing CROs (HLAGAAAE)

Keywords

  • Clinical research services
  • Bioavailability bioequivalence studies
  • Bioanalytical services
  • Clinical data management
  • Contract research organization

Where ClinSync Clinical Research Pvt Ltd is headquartered

Location

Headquarters

HQ city
Hyderabad (Madeenaguda)
HQ country
India
HQ region
Asia

Offices2 records

Markets served

ClinSync Clinical Research Pvt Ltd 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. Clinical Research Services: Fee-for-service B2B model providing end-to-end clinical research services to pharmaceutical, biotech, biosimilar, and medical device companies. Revenue generated through project-based contracts for BA/BE studies, clinical trials, data management, bioanalytical services, and medical writing.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractProject-based service pricing

Go-to-market motion1 record

Distribution channels2 records

Marketing channels6 records

ClinSync Clinical Research Pvt Ltd product offering

Product offering

Core offering

ClinSync Clinical Research Pvt Ltd is a Contract Research Organization that delivers outsourced clinical research services to pharmaceutical, biotechnology, biosimilar, and medical device companies. The company conducts Bioavailability/Bioequivalence (BA/BE) studies, Phase II-IV clinical trials, clinical data management, and bioanalytical laboratory analyses on a fee-for-service basis.

Product overview

ClinSync Clinical Research Pvt Ltd is a Contract Research Organization (CRO) established in 2011 in India, providing comprehensive end-to-end services to pharmaceutical, biotech, biosimilar, and medical device industries. The company operates as a unified platform offering BA/BE Studies (390+ completed), Clinical Trial Operations (Phase II-IV), Clinical Data Management, Bioanalytical Services, Clinical Pharmacology, Pharmacokinetics/Biostatistics, Medical Writing, Cold Chain Management, and Personal Healthcare (FMCG) testing services. With a 160-bed clinical facility and 130+ professionals, the company integrates these services to support drug development from early-phase bioequivalence studies through late-phase clinical trials and regulatory submissions.

Differentiator

Problem solved

Functional benefit

Products and services

  • Bioavailability/Bioequivalence (BA/BE) Studies Conducted for pharmaceutical and biosimilar manufacturers requiring regulatory bioequivalence data for generic drug submissions and comparative pharmacokinetic studies.
  • Clinical Trials (Phase II-IV) Phase II through Phase IV clinical trial design, conduct, and monitoring services for pharmaceutical, biotechnology, and medical device sponsors across multiple therapeutic areas.
  • Clinical Data Management Clinical trial database design, data entry, validation, discrepancy management, and database lock services for sponsors running clinical studies.
  • Bioanalytical Services Laboratory bioanalytical method development, validation, and sample analysis for pharmacokinetic, bioavailability, and bioequivalence studies, supporting both clinical trials and standalone bioanalytical projects.

Quantifiable outcome

  • 390+ BA/BE studies completed
  • +6 more outcomes

Companies that use ClinSync Clinical Research Pvt Ltd

Customer profile

Named customers11 records

Segments4 records

Ideal customer profiles2 records

ClinSync Clinical Research Pvt Ltd technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

ClinSync Clinical Research Pvt Ltd partnerships and signals

Strategic signal

Scale indicators11 records

Recent moves9 records

Expansion highlights5 records

ClinSync Clinical Research Pvt Ltd competitors and assessment

Company assessment

Direct peers

  • Syngene International: India-based integrated CRO/CDMO serving global pharma and biotech with clinical development, bioanalytical, and data management services. Syngene is a direct peer — also a listed ClinSync customer and competitor for outsourced clinical and bioanalytical work out of India.
  • Lambda Therapeutic Research: Indian CRO providing BA/BE, Phase I-IV clinical trials, bioanalytical, and clinical data management services. Lambda is a direct competitor targeting the same generic and biosimilar sponsor base with similar service breadth.
  • Cliantha Research: Indian CRO with multi-therapeutic clinical research, bioanalytical, and dermatology/cosmetics testing capabilities. Cliantha competes with ClinSync in both pharma BA/BE and the Personal Healthcare/FMCG testing vertical ClinSync launched in 2022.
  • Veeda Clinical Research: Indian CRO headquartered in Ahmedabad offering BA/BE studies, bioanalytical services, and clinical research across therapeutic areas. Veeda is one of ClinSync's closest head-to-head competitors for Indian generic sponsor BA/BE and Phase II-IV outsourcing.
  • GVK BIO (Aragen): Hyderabad-headquartered CRO/CDMO offering clinical research, bioanalytical, and discovery services to global pharma. GVK BIO is a directly comparable Indian CRO competing for the same Hyderabad-based sponsor relationships and talent pool.

Broad incumbents

  • Parexel International: Global CRO offering Phase I-IV clinical operations, bioanalytical, regulatory, and post-approval services. Parexel is a broad incumbent competitor for multi-country Phase II-IV and bioequivalence work that large pharma sponsors might award instead of a mid-sized Indian CRO.
  • IQVIA: Global full-service CRO and clinical technology provider. IQVIA is a broad incumbent that competes for the same Phase II-IV clinical trial and bioanalytical work as ClinSync, with substantially larger global footprint, therapeutic breadth, and scale.
  • Labcorp Drug Development (formerly Covance): Global CRO with extensive bioanalytical, central lab, and early-stage clinical capabilities. Labcorp is a broad incumbent that competes for global pharma BA/BE and Phase II-IV work, including USFDA-submission programs that Indian CROs target.
  • Charles River Laboratories: Global CRO providing bioanalytical, safety, and clinical research services. Charles River is a broad incumbent competing for the same regulated bioanalytical and Phase II-IV work, particularly for large pharma and biotech sponsors.

Regional players

  • Pharmaron: China-headquartered CRO/CDMO offering laboratory, bioanalytical, and clinical research services across geographies. Pharmaron is a regional peer — operates in the same Asia-based outsourcing value proposition that Indian CROs like ClinSync compete within for global sponsor BA/BE and clinical work.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

ClinSync Clinical Research Pvt Ltd social profiles

Digital presence

ClinSync Clinical Research Pvt Ltd financial estimates

Financial estimate

Revenue estimate

Valuation estimate

ClinSync Clinical Research Pvt Ltd leadership team

Management profile

Number of profiles

ClinSync Clinical Research Pvt Ltd funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

ClinSync Clinical Research Pvt Ltd 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 ClinSync Clinical Research Pvt Ltd

What does ClinSync Clinical Research Pvt Ltd do?

ClinSync Clinical Research Pvt Ltd is a Contract Research Organization that delivers outsourced clinical research services to pharmaceutical, biotechnology, biosimilar, and medical device companies. The company conducts Bioavailability/Bioequivalence (BA/BE) studies, Phase II-IV clinical trials, clinical data management, and bioanalytical laboratory analyses on a fee-for-service basis.

Is ClinSync Clinical Research Pvt Ltd a public or private company?

ClinSync Clinical Research Pvt Ltd is a private company. It is classified as unknown and is currently operating.

When was ClinSync Clinical Research Pvt Ltd founded?

ClinSync Clinical Research Pvt Ltd was founded in 2011. It employs 101 to 250 people.

Where is ClinSync Clinical Research Pvt Ltd based?

ClinSync Clinical Research Pvt Ltd is headquartered in Hyderabad (Madeenaguda), India, in the Asia region.

How does ClinSync Clinical Research Pvt Ltd make money?

One revenue line is on record: clinical Research Services.

Who are ClinSync Clinical Research Pvt Ltd's main competitors?

Direct peers on record are Syngene International, Lambda Therapeutic Research, Cliantha Research, Veeda Clinical Research and GVK BIO (Aragen). Broad incumbents are Parexel International, IQVIA, Labcorp Drug Development (formerly Covance) and Charles River Laboratories. Pharmaron is listed as a regional player.

Does ClinSync Clinical Research Pvt Ltd have an API?

No public API is recorded for ClinSync Clinical Research Pvt Ltd.

What industry is ClinSync Clinical Research Pvt Ltd in?

ClinSync Clinical Research Pvt Ltd's product category is Contract Research Organization (CRO) Services. Its primary akta.pro industry code is HLAGAAAA, Clinical CROs (Phase I–IV), with a secondary code of HLAGAFAC, DMPK / ADME & Bioanalysis. Its NAICS code is 54171 and its SIC code is 8731.

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