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Promedica International

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uuid000l4bf

Namestring
Promedica International
Legal namestring
Promedica International
Company typeenum
Private
Founded yearint
1984
Descriptiontext

Promedica International is a US-based contract research organization (CRO) specializing exclusively in ophthalmology clinical trials for pharmaceutical, biotechnology, and medical device sponsors. Founded in 1984 and headquartered in Costa Mesa, California, the company operates with a headcount of 11–50 employees across East Coast and West Coast offices, delivering end-to-end trial execution from protocol development through regulatory submission. Its service architecture covers anterior and posterior segment indications, including novel retinal therapies (gene and cell therapy), complex ocular device trials, and programs from early-phase through pivotal stages, supported by an established global investigator network for North American and international delivery.

The firm's go-to-market is a high-touch enterprise sales motion targeting drug and device sponsors, delivered through direct engagement, inside-sales phone contacts, and a B2B content presence via its website and LinkedIn. Its value proposition rests on 100% ophthalmology exclusivity, a regulatory track record of supporting 10 of the 23 FDA-approved ophthalmic drugs since 2008, and a single-vendor lifecycle model that compresses handoffs between design, operations, and regulatory affairs. Revenue mechanics are professional-services engagements scoped by protocol, duration, and complexity; pricing is not publicly disclosed.

In January 2024, Promedica International was acquired by iuvo Bioscience (now operating as iuvo Clinical), forming an end-to-end ophthalmology research platform that spans preclinical development through clinical submission. The combined entity retains Promedica's brand and clinical specialty under a broader strategic acquirer that now provides capital, complementary capabilities, and cross-sell pathways into earlier-stage sponsors—an important context for any evaluation of its standalone trajectory or integration risk.

Short descriptiontext

Promedica International is a US-based, ophthalmology-exclusive contract research organization (CRO) that runs end-to-end clinical trials for pharma, biotech, and ocular-device sponsors, having supported 10 of the 23 FDA-approved ophthalmic drugs since 2008. It was acquired by iuvo Bioscience (now iuvo Clinical) in January 2024.

Operating statusenum
Acquired
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersCosta Mesa, United States
HQ citystring
Costa Mesa
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
ophthalmology clinical trials, contract research organization, clinical trial management, ophthalmic drug development, retinal therapy research
Industry3 codes
1Specialty Therapeutic-Area CROs (e.g., oncology/rare disease)
CodeHLAGAAALPrimaryYes
2Clinical CROs (Phase I–IV)
CodeHLAGAAAAPrimaryNo
3Medical Writing & Regulatory Submission Support CROs
CodeHLAGAAAGPrimaryNo
NAICS code1 code
  • Scientific Research and Development Services5417
Product category
Ophthalmology Contract Research Organization (CRO) Services
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Clinical Research Services
TypeProfessional Services
Description

Contract research organization providing ophthalmology-focused clinical trial management services including protocol development, clinical operations, regulatory affairs, and submission support. Revenue is generated through service contracts with pharmaceutical and biotech sponsors.

iuvoclinical.com
Marketing channels3 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, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

Promedica International (now operating under iuvo Clinical post-acquisition) is an ophthalmology-focused contract research organization (CRO) providing end-to-end clinical trial services to pharmaceutical and biotech sponsors. Services span protocol development, clinical operations, regulatory affairs, and submission support for ophthalmic therapies including novel retinal therapies and complex ocular device trials across anterior and posterior segments.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • Supported 10 of 23 FDA-approved ophthalmic drugs since 2008
Product overview1 text field

Promedica International was a specialized ophthalmology contract research organization that was acquired by Iuvo Bioscience in January 2024. Following the acquisition, the combined entity created an end-to-end ophthalmology research platform spanning preclinical through clinical development stages, with capabilities across anterior and posterior eye segments for retinal therapies and ocular device trials.

Product and service5 records
1End-to-End Clinical Trial Management for Ophthalmology
CategoryClinical Research Organization (CRO) Services
Description

Comprehensive clinical trial management services spanning the full lifecycle of ophthalmic drug and device development for pharmaceutical and biotech sponsors. Includes protocol design, clinical operations, site management, regulatory affairs, and submission support across anterior and posterior segment indications.

2Ophthalmic Drug Clinical Trials (Retinal and Anterior/Posterior Segment)
CategoryClinical Research Organization (CRO) Services
Description

Specialized clinical trial services for novel ophthalmic drug development including retinal therapies, gene therapies, cell therapies, and novel drug delivery systems. Supports early-phase through pivotal trials for sponsors pursuing FDA approval of ophthalmic therapeutics.

3Ocular Medical Device Clinical Trials
CategoryClinical Research Organization (CRO) Services
Description

Clinical trial design and execution services for ocular medical devices requiring regulatory approval, supporting device trial design complexity and global trial execution for medical device companies.

4Regulatory Affairs and Submission Support
CategoryRegulatory Affairs Services
Description

Regulatory affairs services supporting FDA submission for ophthalmic drugs and devices, including regulatory strategy, submission preparation, and FDA interaction support.

5Global Clinical Trial Network Management
CategoryClinical Research Organization (CRO) Services
Description

Management of clinical trials across a global network of sites spanning North America and international locations, while preserving the responsiveness and attention to detail of a focused ophthalmology-only CRO.

Scale indicator2 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-01-01
Description

In January 2024, US-based iuvo Bioscience acquired Promedica International to create an end-to-end ophthalmology research platform spanning preclinical through clinical development stages. This acquisition combined Promedica International's expertise with iuvo's existing capabilities to form a comprehensive ophthalmology CRO offering.

Recent move4 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

World's largest CRO with a dedicated ophthalmology therapeutic center of excellence. Comparable as the broadest incumbent able to bundle ophthalmology with data, RWE, and central lab services.

TypeDirect peer
Description

Mid-size CRO with a dedicated ophthalmology therapeutic area and pediatric/specialty focus. Directly comparable on ophthalmology clinical services and similar sponsor-segment focus.

TypeDirect peer
Description

Mid-size full-service CRO serving biotech and specialty pharma. Comparable as a similarly sized, therapeutic-area-oriented CRO bidding on the same niche sponsor contracts.

TypeBroad incumbent
Description

Preclinical and early-stage CRO with growing clinical services footprint. Comparable given iuvo's preclinical heritage and potential adjacency as the combined platform expands its end-to-end offering.

TypeBroad incumbent
Description

Top global CRO with biotech-focused commercial and clinical offerings including ophthalmology. Comparable as a broad incumbent pursuing the same sponsor relationships at scale.

TypeBroad incumbent
Description

Global top-5 CRO offering full-service clinical development including ophthalmology studies. Comparable as a broad incumbent with dedicated therapeutic units competing for ophthalmology sponsors.

TypeDirect peer
Description

Mid-size full-service CRO with therapeutic-area depth across multiple specialties. Comparable as a similarly-sized CRO competitor pursuing complex, regulated studies for small-to-mid biotech sponsors.

TypeBroad incumbent
Description

Large full-service CRO with strong biotech sponsor base and growing ophthalmology book. Comparable as a larger incumbent expanding into the same specialty clinical trial space.

TypeDirect peer
Description

Specialty ophthalmology CRO offering end-to-end clinical research services to pharma and biotech sponsors. Directly comparable as another boutique, ophthalmology-only CRO competing for the same sponsor programs.

TypeBroad incumbent
Description

Mid-to-large global CRO with therapeutic-area specialization including ophthalmology. Comparable as a broader-scope specialty CRO competitor.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat4 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

Segment2 records

Each record includes

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

Ideal customer profile2 records

Each record includes

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

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 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 →

Promedica International

Ophthalmology Contract Research Organization (CRO) Servicespromedica-intl.com

Promedica International is a US-based, ophthalmology-exclusive contract research organization (CRO) that runs end-to-end clinical trials for pharma, biotech, and ocular-device sponsors, having supported 10 of the 23 FDA-approved ophthalmic drugs since 2008. It was acquired by iuvo Bioscience (now iuvo Clinical) in January 2024.

What Promedica International does

Promedica International is a US-based contract research organization (CRO) specializing exclusively in ophthalmology clinical trials for pharmaceutical, biotechnology, and medical device sponsors. Founded in 1984 and headquartered in Costa Mesa, California, the company operates with a headcount of 11–50 employees across East Coast and West Coast offices, delivering end-to-end trial execution from protocol development through regulatory submission. Its service architecture covers anterior and posterior segment indications, including novel retinal therapies (gene and cell therapy), complex ocular device trials, and programs from early-phase through pivotal stages, supported by an established global investigator network for North American and international delivery.

The firm's go-to-market is a high-touch enterprise sales motion targeting drug and device sponsors, delivered through direct engagement, inside-sales phone contacts, and a B2B content presence via its website and LinkedIn. Its value proposition rests on 100% ophthalmology exclusivity, a regulatory track record of supporting 10 of the 23 FDA-approved ophthalmic drugs since 2008, and a single-vendor lifecycle model that compresses handoffs between design, operations, and regulatory affairs. Revenue mechanics are professional-services engagements scoped by protocol, duration, and complexity; pricing is not publicly disclosed.

In January 2024, Promedica International was acquired by iuvo Bioscience (now operating as iuvo Clinical), forming an end-to-end ophthalmology research platform that spans preclinical development through clinical submission. The combined entity retains Promedica's brand and clinical specialty under a broader strategic acquirer that now provides capital, complementary capabilities, and cross-sell pathways into earlier-stage sponsors—an important context for any evaluation of its standalone trajectory or integration risk.

Promedica International firmographics

Firmographics
Name
Promedica International
Legal name
Promedica International
Website
https://promedica-intl.com
Company type
Private
Founded year
1984
Operating status
Acquired
Headcount range
11–50 employees
Short description
Promedica International is a US-based, ophthalmology-exclusive contract research organization (CRO) that runs end-to-end clinical trials for pharma, biotech, and ocular-device sponsors, having supported 10 of the 23 FDA-approved ophthalmic drugs since 2008. It was acquired by iuvo Bioscience (now iuvo Clinical) in January 2024.
Ownership category
akta.pro rank

Promedica International industry classification

Industry
Product category
Ophthalmology Contract Research Organization (CRO) Services
NAICS
Scientific Research and Development Services (5417)
akta.pro primary industry
Specialty Therapeutic-Area CROs (e.g., oncology/rare disease) (HLAGAAAL)
akta.pro secondary industries
Clinical CROs (Phase I–IV) (HLAGAAAA), Medical Writing & Regulatory Submission Support CROs (HLAGAAAG)

Keywords

  • Ophthalmology clinical trials
  • Contract research organization
  • Clinical trial management
  • Ophthalmic drug development
  • Retinal therapy research

Where Promedica International is headquartered

Location

Headquarters

HQ city
Costa Mesa
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Promedica International business model

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

Revenue model

  1. Clinical Research Services: Contract research organization providing ophthalmology-focused clinical trial management services including protocol development, clinical operations, regulatory affairs, and submission support. Revenue is generated through service contracts with pharmaceutical and biotech sponsors.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels3 records

Promedica International product offering

Product offering

Core offering

Promedica International (now operating under iuvo Clinical post-acquisition) is an ophthalmology-focused contract research organization (CRO) providing end-to-end clinical trial services to pharmaceutical and biotech sponsors. Services span protocol development, clinical operations, regulatory affairs, and submission support for ophthalmic therapies including novel retinal therapies and complex ocular device trials across anterior and posterior segments.

Product overview

Promedica International was a specialized ophthalmology contract research organization that was acquired by Iuvo Bioscience in January 2024. Following the acquisition, the combined entity created an end-to-end ophthalmology research platform spanning preclinical through clinical development stages, with capabilities across anterior and posterior eye segments for retinal therapies and ocular device trials.

Differentiator

Problem solved

Functional benefit

Products and services

  • End-to-End Clinical Trial Management for Ophthalmology Comprehensive clinical trial management services spanning the full lifecycle of ophthalmic drug and device development for pharmaceutical and biotech sponsors. Includes protocol design, clinical operations, site management, regulatory affairs, and submission support across anterior and posterior segment indications.
  • Ophthalmic Drug Clinical Trials (Retinal and Anterior/Posterior Segment) Specialized clinical trial services for novel ophthalmic drug development including retinal therapies, gene therapies, cell therapies, and novel drug delivery systems. Supports early-phase through pivotal trials for sponsors pursuing FDA approval of ophthalmic therapeutics.
  • Ocular Medical Device Clinical Trials Clinical trial design and execution services for ocular medical devices requiring regulatory approval, supporting device trial design complexity and global trial execution for medical device companies.
  • Regulatory Affairs and Submission Support Regulatory affairs services supporting FDA submission for ophthalmic drugs and devices, including regulatory strategy, submission preparation, and FDA interaction support.
  • Global Clinical Trial Network Management Management of clinical trials across a global network of sites spanning North America and international locations, while preserving the responsiveness and attention to detail of a focused ophthalmology-only CRO.

Quantifiable outcome

  • Supported 10 of 23 FDA-approved ophthalmic drugs since 2008

Companies that use Promedica International

Customer profile

Segments2 records

Ideal customer profiles2 records

Promedica International technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Promedica International partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • iuvo BiosciencecoreStrategic or Co-development Partner · 1 January 2024In January 2024, US-based iuvo Bioscience acquired Promedica International to create an end-to-end ophthalmology research platform spanning preclinical through clinical development stages. This acquisition combined Promedica International's expertise with iuvo's existing capabilities to form a comprehensive ophthalmology CRO offering.

Scale indicators2 records

Recent moves4 records

Expansion highlights4 records

Promedica International competitors and assessment

Company assessment

Broad incumbents

  • IQVIA: World's largest CRO with a dedicated ophthalmology therapeutic center of excellence. Comparable as the broadest incumbent able to bundle ophthalmology with data, RWE, and central lab services.
  • Charles River Laboratories: Preclinical and early-stage CRO with growing clinical services footprint. Comparable given iuvo's preclinical heritage and potential adjacency as the combined platform expands its end-to-end offering.
  • Syneos Health: Top global CRO with biotech-focused commercial and clinical offerings including ophthalmology. Comparable as a broad incumbent pursuing the same sponsor relationships at scale.
  • ICON plc: Global top-5 CRO offering full-service clinical development including ophthalmology studies. Comparable as a broad incumbent with dedicated therapeutic units competing for ophthalmology sponsors.
  • Medpace: Large full-service CRO with strong biotech sponsor base and growing ophthalmology book. Comparable as a larger incumbent expanding into the same specialty clinical trial space.
  • Worldwide Clinical Trials: Mid-to-large global CRO with therapeutic-area specialization including ophthalmology. Comparable as a broader-scope specialty CRO competitor.

Direct peers

  • Premier Research: Mid-size CRO with a dedicated ophthalmology therapeutic area and pediatric/specialty focus. Directly comparable on ophthalmology clinical services and similar sponsor-segment focus.
  • Clinipace Worldwide: Mid-size full-service CRO serving biotech and specialty pharma. Comparable as a similarly sized, therapeutic-area-oriented CRO bidding on the same niche sponsor contracts.
  • Rho: Mid-size full-service CRO with therapeutic-area depth across multiple specialties. Comparable as a similarly-sized CRO competitor pursuing complex, regulated studies for small-to-mid biotech sponsors.
  • Ora, Inc. Specialty ophthalmology CRO offering end-to-end clinical research services to pharma and biotech sponsors. Directly comparable as another boutique, ophthalmology-only CRO competing for the same sponsor programs.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks5 records

Key highlights6 records

Customer concentration

Promedica International social profiles

Digital presence

Promedica International financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Promedica International leadership team

Management profile

Number of profiles

Promedica International funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Promedica International 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 Promedica International

What does Promedica International do?

Promedica International (now operating under iuvo Clinical post-acquisition) is an ophthalmology-focused contract research organization (CRO) providing end-to-end clinical trial services to pharmaceutical and biotech sponsors. Services span protocol development, clinical operations, regulatory affairs, and submission support for ophthalmic therapies including novel retinal therapies and complex ocular device trials across anterior and posterior segments.

Is Promedica International a public or private company?

Promedica International is a private company. It is classified as corporate owned and is currently acquired.

When was Promedica International founded?

Promedica International was founded in 1984. It employs 11 to 50 people.

Where is Promedica International based?

Promedica International is headquartered in Costa Mesa, United States, in the North America region.

How does Promedica International make money?

One revenue line is on record: clinical Research Services.

Who are Promedica International's main competitors?

Broad incumbents on record are IQVIA, Charles River Laboratories, Syneos Health, ICON plc, Medpace and Worldwide Clinical Trials. Direct peers are Premier Research, Clinipace Worldwide, Rho and Ora, Inc..

Does Promedica International have an API?

No public API is recorded for Promedica International.

What industry is Promedica International in?

Promedica International's product category is Ophthalmology Contract Research Organization (CRO) Services. Its primary akta.pro industry code is HLAGAAAL, Specialty Therapeutic-Area CROs (e.g., oncology/rare disease), with a secondary code of HLAGAAAA, Clinical CROs (Phase I–IV). Its NAICS code is 5417.

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Live signals
openPR.comOphthalmology Contract Research Organization Market Overview, Key Trends, and Major Player AnalysisThe ophthalmology contract research organization (CRO) market is projected to reach $4.39 billion by 2030, growing at a compound annual growth rate (CAGR) of 8.1%, driven by investments in gene and cell therapies, demand for real-world evidence studies, and digital trial management platforms. In January 2024, US-based Iuvo Bioscience acquired Promedica International to create an end-to-end ophthalmology research platform spanning preclinical through clinical development stages. The market features numerous CRO players including IQVIA Holdings Inc, ICON plc, and Charles River Laboratories, among others providing ophthalmic research services.Contractpharmaiuvo BioScience Acquires Promedica Internationaliuvo BioScience has acquired Promedica International, a California-based clinical research organization specializing in ophthalmology. As part of the transaction, Shannon Stoddard has been appointed President of Clinical Research for the combined entity and will serve on iuvo's Board of Directors. The merger aims to create a larger provider capable of supporting all aspects of ophthalmic clinical research.Ampersandcapitaliuvo BioScience Acquires Promedica International to Expand Ophthalmic Clinical CRO Servicesiuvo BioScience has acquired Promedica International, an ophthalmology-focused clinical CRO, to expand its specialized clinical research services. The combined entity will leverage the expertise of both teams to support end-to-end laboratory and clinical development for ophthalmic and medical device projects. Private equity firm Ampersand Capital Partners backs the transaction, which positions the new organization as a global leader in this niche market.Prwebiuvo BioScience Acquires Promedica International to Expand Ophthalmic Clinical CRO Servicesiuvo BioScience has acquired Promedica International, an ophthalmology-focused clinical CRO, to expand its ophthalmic clinical research services. As part of the transaction, Shannon Stoddard was appointed President of Clinical Research for the combined entity and joined iuvo's Board of Directors.PR NewswireWorldwide Industry for Medical Device & IVD Regulatory Affairs Outsourcing to 2030 - Featuring Promedica International, Covance and Assent Compliance Among OthersResearchAndMarkets.com announced the release of a global market research report covering the medical device and IVD regulatory affairs outsourcing market for the forecast period 2020–2030, providing historical revenue analysis from 2018 and projecting growth trends through the forecast period. The report examines market dynamics, competitive landscape, segmentation by service and software, and regional forecasts across North America, Europe, Asia-Pacific, Latin America, and the Middle East & Africa. Key companies profiled in the competitive landscape include Promedica International, Covance, Assent Compliance Inc, Freyr, ICON plc, and others identified as market players.