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Viedoc

Full company profile

uuid0007v5a

Namestring
Viedoc
Legal namestring
Viedoc Technologies AB
Websiteurl
viedoc.com
Company typeenum
Private
Founded yearint
2003
Descriptiontext

Viedoc Technologies AB is a privately held Swedish eClinical SaaS provider, founded in 2003 by technologists from the CRO community and headquartered in Uppsala. The company sells a modular, cloud-based clinical trial platform whose core modules include Viedoc EDC (Electronic Data Capture), Viedoc ePRO (electronic patient-reported outcomes with the Viedoc Me patient portal), Viedoc Televisits for decentralized trials, Viedoc eTMF (Electronic Trial Master File), Randomization, RTSM (Randomization and Trial Supply Management), Medical Coding, eSignature, and Record Sharing. Recent additions include the Viedoc SDV Manager for risk-based source data verification and DICOM de-identification for medical imaging workflows, all delivered through a browser-based architecture with 99.99% uptime and support for 40+ languages across 75+ countries. The platform is designed for fast deployment, averaging 10 weeks for study build, and targets compliance with 21 CFR Part 11, GDPR, HIPAA, ICH GCP, GAMP 5, CDISC, ISO 27001:2022, SOC 2 Type 2, APPI, and CSA STAR Level 1.

The company serves three primary customer segments — Contract Research Organizations (CROs), pharma and biotech sponsors, and medical device companies — with a secondary base in academic and research institutions. The customer roster spans multiple named CROs (Clinfidence, FGK CRO, LINK Medical, Linical, MDCE CRO, SMERUD, TECRO), pharma sponsors (Dicot Pharma, RHEACELL), medical device firms (Sonex Health, Qmed, Chordate Medical), and academic institutions (University of Oslo). Revenue is generated through a SaaS subscription model with study-based (not per-seat) pricing, modular licensing of features, annual billing, and optional professional services including Certified Designer Training, Study Build, and Customer Success. Distribution is direct enterprise field sales supported by a CRO Partner Directory and wholly-owned sales entities in the US (Raleigh), Japan (Tokyo), China (Shanghai), Vietnam (Hanoi, engineering), and Australia (Melbourne), enabling regional data residency for EU, US, Japan, and China regulatory regimes. The firm is founder-owned, has approximately 140 employees, and has accumulated more than 7,000 studies, 30,000+ sites, and 1.6M+ participants on the platform.

Short descriptiontext

Viedoc Technologies AB, founded 2003 in Uppsala, Sweden, provides a cloud-based modular eClinical SaaS platform — including EDC, ePRO, eTMF, randomization, RTSM, and televisits — serving CROs, pharma and biotech sponsors, medical device firms, and academic institutions across more than 75 countries via study-based subscription pricing.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersUppsala, Sweden
HQ citystring
Uppsala
HQ countrystring
Sweden
HQ regionstring
Europe
Markets served

Serves global market

Offices6 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical trial software, electronic data capture, eClinical platform, patient reported outcomes, trial master file
Industry4 codes
1Electronic Data Capture (EDC) Platforms
CodeHLACAOAAPrimaryYes
2eTMF & Trial Document Management
CodeHLACAOAFPrimaryNo
3Site Data Management Support (EDC/Source/SDV Readiness)
CodeHLAGACALPrimaryNo
4Clinical Trial Monitoring Support (On-site/Remote)
CodeHLAGACAGPrimaryNo
NAICS code1 code
  • Software Publishers5132
SIC code1 code
  • Services-Prepackaged Software7372
Product category
Clinical Trial Management Software (eClinical Platform)
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1SaaS Platform Licensing
TypeSubscription Recurring
Description

Viedoc operates on a SaaS subscription model with modular, study-based pricing. Customers pay for their study rather than per user, with unlimited users included at no extra cost. Features are modular, allowing customers to choose EDC, ePRO, Televisits or other modules as needed.

viedoc.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
Technology or R&D, Personnel, Infrastructure, Marketing or Sales, Operations
Pricing details1 tier
1Modular study-based licensing with optional modules
ModelSubscriptionBilling cadenceAnnual
Notes

Choose modules as needed: EDC, ePRO, Televisits, Randomization, RTSM, Medical Coding, eTMF, eSignature, Record Sharing. Pay for study not users. Unlimited users included.

viedoc.com
GTM typeB2B
B2B
Offering typeSoftware
Software
Brand1 of 8 records shown
1Viedoc Me
Description

Patient portal application for clinical trial participants

viedoc.com
+7 more records
Core offering1 text field

Viedoc provides a cloud-based, modular eClinical SaaS platform that enables pharmaceutical, biotech, medical device, and contract research organizations to run clinical trials end-to-end. Core modules include Electronic Data Capture (EDC), electronic Patient-Reported Outcomes (ePRO), Televisits for decentralized trials, Electronic Trial Master File (eTMF), randomization, RTSM (trial supply management), medical coding, eSignature, and record sharing. The platform is licensed on a study-basis (not per user) with annual subscriptions and includes hosting, backups, support, and regulatory compliance for FDA, EMA, and PMDA submissions.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 7 values shown
  • 98% study-visit compliance achieved by Sonex Health using Viedoc ePRO
+6 more records
Product overview1 text field

Viedoc is a cloud-based eClinical platform providing an integrated suite of clinical trial software solutions. The platform operates on a modular architecture allowing sponsors and CROs to select and combine capabilities including EDC (electronic data capture), ePRO (electronic patient-reported outcomes), Televisits (decentralized trial support), eTMF (trial master file management), Medical Coding, Randomization, RTSM (trial supply management), Record Sharing, and eSignature. Key features include Viedoc SDV Manager for targeted source data verification supporting risk-based quality management, ViedocReports for analytics and exports, and Viedoc Me as a patient-facing portal for remote participation. The platform is designed for rapid deployment with a 10-week study build time average, supports 40+ languages, and maintains compliance with major regulatory frameworks including FDA, EMA, and PMDA.

Product and service11 records
1Viedoc EDC (Electronic Data Capture)
CategoryElectronic Data Capture (EDC)
Description

Browser-based platform for collecting, validating, verifying, and monitoring high-quality clinical trial data in real time, with audit trails and configurable workflows. Designed for sponsors and CROs running clinical studies.

2Viedoc ePRO (Electronic Patient-Reported Outcomes)
CategoryElectronic Patient-Reported Outcomes (ePRO / eCOA)
Description

Patient-facing module enabling direct reporting of outcomes into the platform, eliminating manual data entry delays. Includes the Viedoc Me patient portal for remote participation.

3Viedoc Televisits
CategoryDecentralized Clinical Trials / Televisits
Description

Remote visit capability that brings decentralized participation into trial workflows, enabling clinical observations and patient data capture from any location.

4Viedoc eTMF (Electronic Trial Master File)
CategoryElectronic Trial Master File (eTMF)
Description

Document management system for maintaining trial master file documentation, ensuring organized storage and retrieval of trial documents throughout the study lifecycle.

5Viedoc Medical Coding
CategoryMedical Coding Module
Description

Automated medical coding tool supporting MedDRA and WHO Drug dictionary integration for coding adverse events and medications consistently across studies.

6Viedoc Randomization
CategoryClinical Trial Randomization
Description

Clinical trial randomization software managing subject allocation to treatment arms with configurable randomization configurations.

7Viedoc RTSM (Randomization and Trial Supply Management)
CategoryRandomization and Trial Supply Management (RTSM)
Description

Trial supply management software for managing drug kit allocation, supply logistics, and inventory across investigator sites.

8Viedoc Record Sharing
CategoryClinical Record Sharing
Description

Capability enabling secure sharing of clinical records and data across authorized parties within the trial ecosystem.

9Viedoc eSignature
CategoryElectronic Signature
Description

Electronic signature capability enabling compliant digital signing of documents and forms within the platform, supporting 21 CFR Part 11 compliance.

10Viedoc PMS (Post-Market Surveillance, Japan)
CategoryPost-Market Surveillance (PMS)
Description

Post-market surveillance software designed specifically for the Japanese market, supporting Japan PMDA regulatory requirements for medical devices and pharmaceuticals.

11Viedoc API
CategoryDeveloper API / Integration Platform
Description

Public application programming interface that enables integrations with third-party systems, with accompanying Tech Partnership Directory and Connector Service.

Scale indicator10 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
1Trialt
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-04-03
Description

Strategic collaboration announced April 3, 2026 between Trialt (global CRO specializing in biostatistics and data management) and Viedoc. Partnership combines Viedoc's technology platform with Trialt's biometrics expertise to help sponsors accelerate clinical trial timelines, strengthen data quality, and improve decision-making. Supports global and decentralized trials with goal of connected experience from data capture through analysis.

einpresswire.com
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-12-15
Description

Strategic partnership announced December 15, 2025 to enhance eClinical services for clinical trials. Collaboration combines Viedoc's platform with Studion's expertise to improve study quality, speed, and data integrity. Partnership aims to support sponsors and CROs in executing faster, more reliable clinical research.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeEmerging player
Description

Medable is a leading decentralized clinical trial platform offering eCOA, eConsent, telehealth, and remote monitoring. It overlaps with Viedoc's Televisits, ePRO, and DCT modules and is a credible competitor for DCT-focused RFPs.

TypeDirect peer
Description

Signant Health (combining CRF Health and Bracket) provides eCOA, EDC, patient engagement, and rater training for clinical trials. It directly competes with Viedoc in ePRO, EDC, and decentralized trial enablement.

TypeBroad incumbent
Description

Clario (formed from ERT and Bioclinica) provides eCOA, EDC, cardiac safety, medical imaging, and trial endpoint solutions to pharma sponsors. It competes with Viedoc across ePRO, EDC, and imaging-adjacent workflows including DICOM handling.

TypeDirect peer
Description

Medrio provides cloud-based EDC, ePRO, eConsent, and RTSM solutions for clinical trials, especially for early-phase and post-market studies. It competes with Viedoc for mid-market and academic customers.

TypeBroad incumbent
Description

Veeva's Vault Clinical Suite includes Vault EDC, Vault CTMS, Vault CDB, and ePRO capabilities targeting large pharma sponsors. Its broad life-sciences CRM and content footprint make it a direct competitor for enterprise clinical platform deals.

TypeEmerging player
Description

Science 37 operates a decentralized clinical trial operating system with integrated telemedicine, eCOA, and connected devices. It competes with Viedoc's DCT and Televisits capabilities, particularly for fully decentralized sponsor studies.

TypeBroad incumbent
Description

Oracle's Clinical One platform unifies EDC, RTSM, ePRO, and trial design under one cloud platform. As a large enterprise software vendor, it competes head-to-head with Viedoc in mid-to-large pharma trials.

TypeBroad incumbent
Description

Medidata offers the industry-leading Rave EDC platform plus a broad clinical cloud suite (CTMS, eCOA, RTSM, imaging, analytics). It is the dominant incumbent against which Viedoc competes for sponsor and CRO EDC RFPs.

TypeDirect peer
Description

OpenClinica offers EDC, ePRO, and clinical data management software for academic and commercial trials. It is a comparable mid-sized cloud EDC vendor competing in similar customer segments.

TypeDirect peer
Description

Castor is a cloud-native EDC and ePRO platform targeting academic, CRO, and small/mid-pharma sponsors with modular pricing. It overlaps directly with Viedoc in EDC, ePRO, and decentralized trial functionality.

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 customers13 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 profile4 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
Yes
API detail
Has APIbool
Yes

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
Profiles7 records

Each record includes

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

Subsidiaries4 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance11 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 →

Viedoc

Clinical Trial Management Software (eClinical Platform)viedoc.com

Viedoc Technologies AB, founded 2003 in Uppsala, Sweden, provides a cloud-based modular eClinical SaaS platform — including EDC, ePRO, eTMF, randomization, RTSM, and televisits — serving CROs, pharma and biotech sponsors, medical device firms, and academic institutions across more than 75 countries via study-based subscription pricing.

What Viedoc does

Viedoc Technologies AB is a privately held Swedish eClinical SaaS provider, founded in 2003 by technologists from the CRO community and headquartered in Uppsala. The company sells a modular, cloud-based clinical trial platform whose core modules include Viedoc EDC (Electronic Data Capture), Viedoc ePRO (electronic patient-reported outcomes with the Viedoc Me patient portal), Viedoc Televisits for decentralized trials, Viedoc eTMF (Electronic Trial Master File), Randomization, RTSM (Randomization and Trial Supply Management), Medical Coding, eSignature, and Record Sharing. Recent additions include the Viedoc SDV Manager for risk-based source data verification and DICOM de-identification for medical imaging workflows, all delivered through a browser-based architecture with 99.99% uptime and support for 40+ languages across 75+ countries. The platform is designed for fast deployment, averaging 10 weeks for study build, and targets compliance with 21 CFR Part 11, GDPR, HIPAA, ICH GCP, GAMP 5, CDISC, ISO 27001:2022, SOC 2 Type 2, APPI, and CSA STAR Level 1.

The company serves three primary customer segments — Contract Research Organizations (CROs), pharma and biotech sponsors, and medical device companies — with a secondary base in academic and research institutions. The customer roster spans multiple named CROs (Clinfidence, FGK CRO, LINK Medical, Linical, MDCE CRO, SMERUD, TECRO), pharma sponsors (Dicot Pharma, RHEACELL), medical device firms (Sonex Health, Qmed, Chordate Medical), and academic institutions (University of Oslo). Revenue is generated through a SaaS subscription model with study-based (not per-seat) pricing, modular licensing of features, annual billing, and optional professional services including Certified Designer Training, Study Build, and Customer Success. Distribution is direct enterprise field sales supported by a CRO Partner Directory and wholly-owned sales entities in the US (Raleigh), Japan (Tokyo), China (Shanghai), Vietnam (Hanoi, engineering), and Australia (Melbourne), enabling regional data residency for EU, US, Japan, and China regulatory regimes. The firm is founder-owned, has approximately 140 employees, and has accumulated more than 7,000 studies, 30,000+ sites, and 1.6M+ participants on the platform.

Viedoc firmographics

Firmographics
Name
Viedoc
Legal name
Viedoc Technologies AB
Website
https://viedoc.com
Company type
Private
Founded year
2003
Operating status
Operating
Headcount range
101–250 employees
Short description
Viedoc Technologies AB, founded 2003 in Uppsala, Sweden, provides a cloud-based modular eClinical SaaS platform — including EDC, ePRO, eTMF, randomization, RTSM, and televisits — serving CROs, pharma and biotech sponsors, medical device firms, and academic institutions across more than 75 countries via study-based subscription pricing.
Ownership category
akta.pro rank

Viedoc industry classification

Industry
Product category
Clinical Trial Management Software (eClinical Platform)
NAICS
Software Publishers (5132)
SIC
Services-Prepackaged Software (7372)
akta.pro primary industry
Electronic Data Capture (EDC) Platforms (HLACAOAA)
akta.pro secondary industries
eTMF & Trial Document Management (HLACAOAF), Site Data Management Support (EDC/Source/SDV Readiness) (HLAGACAL), Clinical Trial Monitoring Support (On-site/Remote) (HLAGACAG)

Keywords

  • Clinical trial software
  • Electronic data capture
  • EClinical platform
  • Patient reported outcomes
  • Trial master file

Where Viedoc is headquartered

Location

Headquarters

HQ city
Uppsala
HQ country
Sweden
HQ region
Europe

Offices6 records

Markets served

Viedoc business model

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

Revenue model

  1. SaaS Platform Licensing: Viedoc operates on a SaaS subscription model with modular, study-based pricing. Customers pay for their study rather than per user, with unlimited users included at no extra cost. Features are modular, allowing customers to choose EDC, ePRO, Televisits or other modules as needed.

Pricing tiers

ModelBillingPrice
SubscriptionAnnualModular study-based licensing with optional modules

Go-to-market motion1 record

Distribution channels2 records

Marketing channels6 records

Viedoc product offering

Product offering

Core offering

Viedoc provides a cloud-based, modular eClinical SaaS platform that enables pharmaceutical, biotech, medical device, and contract research organizations to run clinical trials end-to-end. Core modules include Electronic Data Capture (EDC), electronic Patient-Reported Outcomes (ePRO), Televisits for decentralized trials, Electronic Trial Master File (eTMF), randomization, RTSM (trial supply management), medical coding, eSignature, and record sharing. The platform is licensed on a study-basis (not per user) with annual subscriptions and includes hosting, backups, support, and regulatory compliance for FDA, EMA, and PMDA submissions.

Product overview

Viedoc is a cloud-based eClinical platform providing an integrated suite of clinical trial software solutions. The platform operates on a modular architecture allowing sponsors and CROs to select and combine capabilities including EDC (electronic data capture), ePRO (electronic patient-reported outcomes), Televisits (decentralized trial support), eTMF (trial master file management), Medical Coding, Randomization, RTSM (trial supply management), Record Sharing, and eSignature. Key features include Viedoc SDV Manager for targeted source data verification supporting risk-based quality management, ViedocReports for analytics and exports, and Viedoc Me as a patient-facing portal for remote participation. The platform is designed for rapid deployment with a 10-week study build time average, supports 40+ languages, and maintains compliance with major regulatory frameworks including FDA, EMA, and PMDA.

Differentiator

Problem solved

Functional benefit

Brands

  • Viedoc Me: Patient portal application for clinical trial participants
  • Viedoc Designer
  • Viedoc Clinic
  • Viedoc EDC
  • Viedoc ePRO
  • Viedoc eTMF
  • ViedocReports
  • Viedoc API

Products and services

  • Viedoc EDC (Electronic Data Capture) Browser-based platform for collecting, validating, verifying, and monitoring high-quality clinical trial data in real time, with audit trails and configurable workflows. Designed for sponsors and CROs running clinical studies.
  • Viedoc ePRO (Electronic Patient-Reported Outcomes) Patient-facing module enabling direct reporting of outcomes into the platform, eliminating manual data entry delays. Includes the Viedoc Me patient portal for remote participation.
  • Viedoc Televisits Remote visit capability that brings decentralized participation into trial workflows, enabling clinical observations and patient data capture from any location.
  • Viedoc eTMF (Electronic Trial Master File) Document management system for maintaining trial master file documentation, ensuring organized storage and retrieval of trial documents throughout the study lifecycle.
  • Viedoc Medical Coding Automated medical coding tool supporting MedDRA and WHO Drug dictionary integration for coding adverse events and medications consistently across studies.
  • Viedoc Randomization Clinical trial randomization software managing subject allocation to treatment arms with configurable randomization configurations.
  • Viedoc RTSM (Randomization and Trial Supply Management) Trial supply management software for managing drug kit allocation, supply logistics, and inventory across investigator sites.
  • Viedoc Record Sharing Capability enabling secure sharing of clinical records and data across authorized parties within the trial ecosystem.
  • Viedoc eSignature Electronic signature capability enabling compliant digital signing of documents and forms within the platform, supporting 21 CFR Part 11 compliance.
  • Viedoc PMS (Post-Market Surveillance, Japan) Post-market surveillance software designed specifically for the Japanese market, supporting Japan PMDA regulatory requirements for medical devices and pharmaceuticals.
  • Viedoc API Public application programming interface that enables integrations with third-party systems, with accompanying Tech Partnership Directory and Connector Service.

Quantifiable outcome

  • 98% study-visit compliance achieved by Sonex Health using Viedoc ePRO
  • +6 more outcomes

Companies that use Viedoc

Customer profile

Named customers13 records

Segments4 records

Ideal customer profiles4 records

Viedoc technology and API

Technology

Technology focussed Yes

API detail

Has API
Yes
API docs
API detail

Core technology

AI maturity

App detail

Feature9 records

Viedoc partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered core.

  • TrialtcoreStrategic or Co-development Partner · 3 April 2026Strategic collaboration announced April 3, 2026 between Trialt (global CRO specializing in biostatistics and data management) and Viedoc. Partnership combines Viedoc's technology platform with Trialt's biometrics expertise to help sponsors accelerate clinical trial timelines, strengthen data quality, and improve decision-making. Supports global and decentralized trials with goal of connected experience from data capture through analysis.
  • StudioncoreStrategic or Co-development Partner · 15 December 2025Strategic partnership announced December 15, 2025 to enhance eClinical services for clinical trials. Collaboration combines Viedoc's platform with Studion's expertise to improve study quality, speed, and data integrity. Partnership aims to support sponsors and CROs in executing faster, more reliable clinical research.

Scale indicators10 records

Recent moves6 records

Expansion highlights5 records

Viedoc competitors and assessment

Company assessment

Emerging players

  • Medable: Medable is a leading decentralized clinical trial platform offering eCOA, eConsent, telehealth, and remote monitoring. It overlaps with Viedoc's Televisits, ePRO, and DCT modules and is a credible competitor for DCT-focused RFPs.
  • Science 37: Science 37 operates a decentralized clinical trial operating system with integrated telemedicine, eCOA, and connected devices. It competes with Viedoc's DCT and Televisits capabilities, particularly for fully decentralized sponsor studies.

Direct peers

  • Signant Health: Signant Health (combining CRF Health and Bracket) provides eCOA, EDC, patient engagement, and rater training for clinical trials. It directly competes with Viedoc in ePRO, EDC, and decentralized trial enablement.
  • Medrio: Medrio provides cloud-based EDC, ePRO, eConsent, and RTSM solutions for clinical trials, especially for early-phase and post-market studies. It competes with Viedoc for mid-market and academic customers.
  • OpenClinica: OpenClinica offers EDC, ePRO, and clinical data management software for academic and commercial trials. It is a comparable mid-sized cloud EDC vendor competing in similar customer segments.
  • Castor EDC: Castor is a cloud-native EDC and ePRO platform targeting academic, CRO, and small/mid-pharma sponsors with modular pricing. It overlaps directly with Viedoc in EDC, ePRO, and decentralized trial functionality.

Broad incumbents

  • Clario: Clario (formed from ERT and Bioclinica) provides eCOA, EDC, cardiac safety, medical imaging, and trial endpoint solutions to pharma sponsors. It competes with Viedoc across ePRO, EDC, and imaging-adjacent workflows including DICOM handling.
  • Veeva Systems: Veeva's Vault Clinical Suite includes Vault EDC, Vault CTMS, Vault CDB, and ePRO capabilities targeting large pharma sponsors. Its broad life-sciences CRM and content footprint make it a direct competitor for enterprise clinical platform deals.
  • Oracle Clinical One: Oracle's Clinical One platform unifies EDC, RTSM, ePRO, and trial design under one cloud platform. As a large enterprise software vendor, it competes head-to-head with Viedoc in mid-to-large pharma trials.
  • Medidata (Dassault Systèmes): Medidata offers the industry-leading Rave EDC platform plus a broad clinical cloud suite (CTMS, eCOA, RTSM, imaging, analytics). It is the dominant incumbent against which Viedoc competes for sponsor and CRO EDC RFPs.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

Viedoc social profiles

Digital presence

Viedoc compliance and trust

Trust signal

Compliance11 records

Viedoc financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Viedoc leadership team

Management profile

Number of profiles

Profiles7 records

Viedoc subsidiaries and ownership

Company hierarchy

Subsidiaries4 records

Viedoc funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Viedoc 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 Viedoc

What does Viedoc do?

Viedoc provides a cloud-based, modular eClinical SaaS platform that enables pharmaceutical, biotech, medical device, and contract research organizations to run clinical trials end-to-end. Core modules include Electronic Data Capture (EDC), electronic Patient-Reported Outcomes (ePRO), Televisits for decentralized trials, Electronic Trial Master File (eTMF), randomization, RTSM (trial supply management), medical coding, eSignature, and record sharing. The platform is licensed on a study-basis (not per user) with annual subscriptions and includes hosting, backups, support, and regulatory compliance for FDA, EMA, and PMDA submissions.

Is Viedoc a public or private company?

Viedoc is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was Viedoc founded?

Viedoc was founded in 2003. It employs 101 to 250 people.

Where is Viedoc based?

Viedoc is headquartered in Uppsala, Sweden, in the Europe region.

How does Viedoc make money?

One revenue line is on record: saaS Platform Licensing.

Who are Viedoc's main competitors?

Emerging players on record are Medable and Science 37. Direct peers are Signant Health, Medrio, OpenClinica and Castor EDC. Broad incumbents are Clario, Veeva Systems, Oracle Clinical One and Medidata (Dassault Systèmes).

Does Viedoc have an API?

Yes. Viedoc offers a public API that enables integrations with third-party systems. The platform includes a Tech Partnership Directory for discovering integrations and a Connector Service for linking external tools. Developer documentation is at www.viedoc.com/viedoc-api.

What industry is Viedoc in?

Viedoc's product category is Clinical Trial Management Software (eClinical Platform). Its primary akta.pro industry code is HLACAOAA, Electronic Data Capture (EDC) Platforms, with a secondary code of HLACAOAF, eTMF & Trial Document Management. Its NAICS code is 5132 and its SIC code is 7372.

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EIN PresswireThe Top Clinical Trial Management Software According to the FeaturedCustomers Summer 2026 Customer Success ReportFeaturedCustomers released its Summer 2026 Clinical Trial Management Software Customer Success Report, ranking vendors by customer reference content. Market Leaders include Advarra, ArisGlobal, IQVIA, Medidata, and Veeva; Top Performers include Castor EDC, CRIO, and others; Rising Stars include CliniOps, Crucial Data Solutions, and Ennov. The report is based on over 2,000 verified customer references.EIN PresswireTrialt and Viedoc Partner to Deliver Smarter, Faster Clinical Trial Outcomes Through Connected Data and BiometricsTrialt, a global clinical research organization specializing in biostatistics and data management, announced a strategic collaboration with Viedoc, a provider of cloud-based eClinical solutions, on April 3, 2026. The partnership combines Viedoc's technology platform with Trialt's biometrics expertise to help sponsors accelerate clinical trial timelines, strengthen data quality, and improve decision-making across studies. The collaboration supports a range of studies including global and decentralized trials, with the goal of creating a more connected experience from data capture through analysis.YahooStudion and Viedoc Announce Strategic Partnership for eClinical ExcellenceStudion, an eClinical tech services firm, has joined Viedoc's Partnership Program to provide Viedoc customers with eClinical expertise for clinical trials. The partnership combines Viedoc's eClinical platform with Studion's delivery assurance approach, aiming to help sponsors and CROs achieve faster, more reliable study outcomes. Both companies will collaborate through Viedoc's growing CRO Program.Business Wire BlogStudion and Viedoc Announce Strategic Partnership for eClinical ExcellenceStudion and Viedoc have formed a strategic partnership to enhance eClinical technology services for clinical trials. This collaboration aims to empower Viedoc customers and improve the efficacy and reliability of clinical studies, leveraging Studion's experience from over 2,000 clinical trials. The partnership indicates a focus on delivering high-quality, lower-risk study outcomes for sponsors and CROs.ViedoceClinical Trial Data Management Solution – ViedocViedoc is promoting its eClinical data management platform, a SaaS solution designed to streamline clinical trial data capture and reporting for pharmaceutical and biotech companies. The company highlights that its system has been utilized in over 7,000 studies across more than 75 countries with a stated 99.99% uptime.CcrpsDirectory of Electronic Patient-Reported Outcomes ePRO Tools 2025 EditionThis article presents a 2025 directory of Electronic Patient-Reported Outcomes (ePRO) tools, highlighting their critical role in modernizing clinical trials through real-time data collection and improved patient engagement. It details key platforms such as Medidata, Castor, and Viedoc, while outlining the regulatory requirements like 21 CFR Part 11 and GDPR that govern these systems. The piece also promotes the Advanced Clinical Research Associate Certification (ACRAC) by CCRPS as a training resource for professionals managing ePRO deployments.Clinical Trials ArenaThe future of eClinical technology interoperability: Have your sayViedoc is conducting a comprehensive survey to gather expert insights on eClinical technology interoperability and industry expectations. The initiative seeks feedback from clinical research organizations, pharmaceutical companies, biotech firms, and regulatory bodies to inform the company's product development strategies.