Developer docs
API playgroundTry for free, no card

Search company profiles

European Reference Network

Full company profile

uuid0037cuu

Namestring
European Reference Network
Websiteurl
endo-ern.eu
Company typeenum
Private
Founded yearint
2017
Descriptiontext

European Reference Network is a healthcare organization headquartered in Amsterdam, Netherlands, founded in 2017 with a workforce of 11-50 employees. Its described function is to support patients with rare hormonal disorders through education and training, operating under the domain endo-ern.eu. The entity falls within the broader category of European Reference Networks, which are formalized cross-border healthcare coordination bodies in Europe focused on rare and complex conditions where patient numbers at any single national level are insufficient to develop meaningful clinical expertise.

The source data does not disclose revenue model, pricing, products, technology stack, customer list, funding rounds, management team, partnerships, regulatory actions, or geographic scope beyond the Amsterdam base. The supplied webpage content is a non-substantive loader/verification page containing no extractable product, service, or operational detail. Consequently, the underlying mechanics of how the organization is structured (member hospital network versus service provider), how it is funded (EU grant versus commercial), and how it delivers its education and training function are not established by the available evidence.

Given the absence of commercial signals and the explicit educational/coordinating mission, the organization's business character is more consistent with a publicly funded or quasi-public coordination entity than a venture-backed commercial venture, though the input characterizes it as for_profit. The 11-50 employee scale is small but plausible for a network coordination hub, and the 2017 founding aligns with the first operational wave of formally designated European Reference Networks across the EU. Until primary-source disclosure of revenue model, customer relationships, and funding structure becomes available, the investable profile of this entity cannot be rigorously characterized.

Short descriptiontext

European Reference Network is an Amsterdam-based healthcare organization, founded in 2017, that supports patients with rare hormonal disorders across Europe through education and training of clinical providers.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersAmsterdam, Netherlands
HQ citystring
Amsterdam
HQ countrystring
Netherlands
HQ regionstring
Europe
Markets served

Serves global market

Keyword5 values
rare disease networks, endocrine disorder care, medical education training, healthcare referral networks, rare hormonal disorders
Industry1 code
1Rare Disease & Special Needs Support Organizations
CodeBPAGACAMPrimaryYes
NAICS code1 code
  • Other Individual and Family Services62419
SIC code1 code
  • Services-Misc Health & Allied Services, Nec8090
Product category
Rare Disease Healthcare Networks
Cost components5 values
Personnel, Operations, Technology or R&D, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

European Reference Network is a healthcare network that supports patients with rare hormonal disorders. It operates by connecting specialists and reference centers, and delivers education and training to clinicians managing rare endocrine conditions. The core service is healthcare network coordination combined with clinical education on rare hormonal disorders.

Differentiator
Functional benefit
Problem solved
Product and service1 record
1Education and Training Programs on Rare Endocrine Disorders
Recent move1 record

Each record includes

Date, Type, Title, Description, Source

Expansion highlight1 record

Each record includes

Type, Description

Peers10 records
TypeRegional player
Description

European partnership of public health bodies and NGOs; comparable as a Brussels-anchored health-network coordinator that operates across multiple EU member states, though with a broader public-health remit than the subject company.

TypeDirect peer
Description

Global alliance of rare-disease patient organizations; comparable as a coordinating and policy-advocacy body serving rare-disease communities with a similar mission profile to Endo-ERN.

TypeDirect peer
Description

Pan-European specialty society for endocrinology; highly comparable as an educator and convenor for the same clinical community the subject company's training programs serve.

TypeDirect peer
Description

Reference portal and knowledge base for rare diseases including rare endocrine conditions; directly comparable as a European rare-disease information and classification network serving clinicians and patients.

TypeBroad incumbent
Description

Larger, well-established US-based rare-disease umbrella organization; comparable mission and patient-support model but broader disease scope and larger operating footprint than the subject company.

TypeDirect peer
Description

US-based rare-disease advocacy and education non-profit; comparable as a content, education, and patient-support organization focused on rare-disease awareness and clinician resources.

TypeDirect peer
Description

A sister European Reference Network focused on rare hematological diseases; structurally identical in setup, EU funding model, and clinician-coordination mandate, making it the closest like-for-like comparator.

TypeDirect peer
Description

Subspecialty society covering pediatric endocrine disorders, a core area of the subject company's scope; competes for the same clinician training and guideline authority in overlapping rare pediatric conditions.

TypeDirect peer
Description

Moderated online community for rare-disease patients and families; comparable as a peer-led rare-disease support and educational platform overlapping the patient-community mission.

TypeDirect peer
Description

European Organisation for Rare Diseases umbrella advocacy group; comparable as a pan-European non-profit operating across many rare disease communities with overlapping patient and policy stakeholders.

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 highlights5 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

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

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 →

European Reference Network

Rare Disease Healthcare Networksendo-ern.eu

European Reference Network is an Amsterdam-based healthcare organization, founded in 2017, that supports patients with rare hormonal disorders across Europe through education and training of clinical providers.

What European Reference Network does

European Reference Network is a healthcare organization headquartered in Amsterdam, Netherlands, founded in 2017 with a workforce of 11-50 employees. Its described function is to support patients with rare hormonal disorders through education and training, operating under the domain endo-ern.eu. The entity falls within the broader category of European Reference Networks, which are formalized cross-border healthcare coordination bodies in Europe focused on rare and complex conditions where patient numbers at any single national level are insufficient to develop meaningful clinical expertise.

The source data does not disclose revenue model, pricing, products, technology stack, customer list, funding rounds, management team, partnerships, regulatory actions, or geographic scope beyond the Amsterdam base. The supplied webpage content is a non-substantive loader/verification page containing no extractable product, service, or operational detail. Consequently, the underlying mechanics of how the organization is structured (member hospital network versus service provider), how it is funded (EU grant versus commercial), and how it delivers its education and training function are not established by the available evidence.

Given the absence of commercial signals and the explicit educational/coordinating mission, the organization's business character is more consistent with a publicly funded or quasi-public coordination entity than a venture-backed commercial venture, though the input characterizes it as for_profit. The 11-50 employee scale is small but plausible for a network coordination hub, and the 2017 founding aligns with the first operational wave of formally designated European Reference Networks across the EU. Until primary-source disclosure of revenue model, customer relationships, and funding structure becomes available, the investable profile of this entity cannot be rigorously characterized.

European Reference Network firmographics

Firmographics
Name
European Reference Network
Website
https://endo-ern.eu
Company type
Private
Founded year
2017
Operating status
Operating
Headcount range
11–50 employees
Short description
European Reference Network is an Amsterdam-based healthcare organization, founded in 2017, that supports patients with rare hormonal disorders across Europe through education and training of clinical providers.
Ownership category
akta.pro rank

European Reference Network industry classification

Industry
Product category
Rare Disease Healthcare Networks
NAICS
Other Individual and Family Services (62419)
SIC
Services-Misc Health & Allied Services, Nec (8090)
akta.pro primary industry
Rare Disease & Special Needs Support Organizations (BPAGACAM)

Keywords

  • Rare disease networks
  • Endocrine disorder care
  • Medical education training
  • Healthcare referral networks
  • Rare hormonal disorders

Where European Reference Network is headquartered

Location

Headquarters

HQ city
Amsterdam
HQ country
Netherlands
HQ region
Europe

Markets served

European Reference Network business model

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

European Reference Network product offering

Product offering

Core offering

European Reference Network is a healthcare network that supports patients with rare hormonal disorders. It operates by connecting specialists and reference centers, and delivers education and training to clinicians managing rare endocrine conditions. The core service is healthcare network coordination combined with clinical education on rare hormonal disorders.

Differentiator

Problem solved

Functional benefit

Products and services

  • Education and Training Programs on Rare Endocrine Disorders

Companies that use European Reference Network

Customer profile

Ideal customer profiles2 records

European Reference Network technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

European Reference Network partnerships and signals

Strategic signal

Recent moves1 record

Expansion highlights1 record

European Reference Network competitors and assessment

Company assessment

Regional players

  • EuroHealthNet: European partnership of public health bodies and NGOs; comparable as a Brussels-anchored health-network coordinator that operates across multiple EU member states, though with a broader public-health remit than the subject company.

Direct peers

  • Rare Diseases International: Global alliance of rare-disease patient organizations; comparable as a coordinating and policy-advocacy body serving rare-disease communities with a similar mission profile to Endo-ERN.
  • European Society of Endocrinology: Pan-European specialty society for endocrinology; highly comparable as an educator and convenor for the same clinical community the subject company's training programs serve.
  • Orphanet: Reference portal and knowledge base for rare diseases including rare endocrine conditions; directly comparable as a European rare-disease information and classification network serving clinicians and patients.
  • Global Genes: US-based rare-disease advocacy and education non-profit; comparable as a content, education, and patient-support organization focused on rare-disease awareness and clinician resources.
  • ERN-EuroBloodNet: A sister European Reference Network focused on rare hematological diseases; structurally identical in setup, EU funding model, and clinician-coordination mandate, making it the closest like-for-like comparator.
  • European Society for Paediatric Endocrinology: Subspecialty society covering pediatric endocrine disorders, a core area of the subject company's scope; competes for the same clinician training and guideline authority in overlapping rare pediatric conditions.
  • RareConnect: Moderated online community for rare-disease patients and families; comparable as a peer-led rare-disease support and educational platform overlapping the patient-community mission.
  • EURORDIS: European Organisation for Rare Diseases umbrella advocacy group; comparable as a pan-European non-profit operating across many rare disease communities with overlapping patient and policy stakeholders.

Broad incumbents

  • NORD (National Organization for Rare Disorders): Larger, well-established US-based rare-disease umbrella organization; comparable mission and patient-support model but broader disease scope and larger operating footprint than the subject company.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks5 records

Key highlights5 records

Customer concentration

European Reference Network social profiles

Digital presence

European Reference Network financial estimates

Financial estimate

Revenue estimate

Valuation estimate

European Reference Network leadership team

Management profile

Number of profiles

European Reference Network funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

European Reference Network 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 European Reference Network

What does European Reference Network do?

European Reference Network is a healthcare network that supports patients with rare hormonal disorders. It operates by connecting specialists and reference centers, and delivers education and training to clinicians managing rare endocrine conditions. The core service is healthcare network coordination combined with clinical education on rare hormonal disorders.

When was European Reference Network founded?

European Reference Network was founded in 2017. It employs 11 to 50 people.

Where is European Reference Network based?

European Reference Network is headquartered in Amsterdam, Netherlands, in the Europe region.

Who are European Reference Network's main competitors?

EuroHealthNet is listed as a regional player. Direct peers are Rare Diseases International, European Society of Endocrinology, Orphanet, Global Genes, ERN-EuroBloodNet, European Society for Paediatric Endocrinology, RareConnect and EURORDIS. NORD (National Organization for Rare Disorders) is listed as a broad incumbent.

Does European Reference Network have an API?

No public API is recorded for European Reference Network.

What industry is European Reference Network in?

European Reference Network's product category is Rare Disease Healthcare Networks. Its primary akta.pro industry code is BPAGACAM, Rare Disease & Special Needs Support Organizations. Its NAICS code is 62419 and its SIC code is 8090.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales