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Cevidra

Full company profile

uuid000slz5

Namestring
Cevidra
Legal namestring
Cevidra
Websiteurl
cevidra.com
Company typeenum
Private
Founded yearint
2006
Descriptiontext

Cevidra is a privately-held French pharmaceutical services firm headquartered in Grasse, France, founded in 2006 and operating with 11–50 employees under founder-CEO Stephane Destaing. The company operates as an Exploitant, a regulated status that legally allows it to market and distribute medicinal products in France on behalf of Marketing Authorization Holders not established in France. It provides an integrated continuum of pharmaceutical services — Early Access Programs, Compassionate Use / Named Patient Programs, Market Access, Post-Market Surveillance, Supply Chain Optimization, Promotion & Sales, and Regulatory Compliance — targeted at international and domestic pharmaceutical, biotech, ATMP, blood-product, and orphan-drug developers seeking entry into the French hospital market.

Cevidra's offerings are specialized around high-value, regulated therapeutic categories: blood-derived products, Advanced Therapy Medicinal Products (cell and gene therapies), and orphan drugs for rare diseases. Operationally, the firm maintains direct relationships with major French public hospital purchasing platforms (including RESPAN and UNIHA), responds to public tenders for hospital procurement, runs a 24/7 distribution operation with same-day shipping for orders placed before 4 p.m. and next-day delivery, and provides secondary packaging and batch release services. Pharmacist-led teams handle quality complaints, medical information requests, pharmacovigilance, and post-market surveillance. Industry association memberships (MabDesign, Eurobiomed, EUCOPE, AMLIS) embed Cevidra in the French and European biotherapy and SME health ecosystems.

Cevidra is a B2B professional-services business with quote-based, scope-dependent pricing; revenue mechanics are not publicly disclosed. The firm generates revenue across multiple customer segments — pharmaceutical manufacturers, biotech firms, ATMP developers, orphan-drug manufacturers, and blood-product companies — but is geographically concentrated entirely in France (Europe). There are no disclosed funding rounds, no parent company, and no indications of external private equity or venture capital backing; Cevidra appears to be an independent, founder/management-owned private company.

Short descriptiontext

Cevidra is a French pharmaceutical services firm that acts as a regulated Exploitant, providing early access, market access, supply chain, and post-market surveillance services for high-value hospital drugs, including ATMPs, orphan drugs, and blood-derived products, primarily serving international and domestic pharma manufacturers entering the French hospital market.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersGrasse, France
HQ citystring
Grasse
HQ countrystring
France
HQ regionstring
Europe
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
pharmaceutical regulatory services, early access programs, orphan drug market access, hospital drug distribution, ATMP commercialization
NAICS code1 code
  • Other Scientific and Technical Consulting Services54169
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Pharmaceutical Regulatory Services
No data
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Services
TypeProfessional Services
Description

Cevidra generates revenue through comprehensive pharmaceutical services including early access programs, compassionate use programs, market access consulting, regulatory compliance, supply chain optimization, and promotion & sales services for medicinal products targeting the French hospital market.

cevidra.com
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Operations, Marketing or Sales, Technology or R&D, Others
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

Cevidra is a French pharmaceutical services company founded in 2006 and based in Grasse, France. The company provides regulatory and operational support for marketing high-value drugs intended for hospital use in France, holding the Exploitant status required by French authorities. Cevidra specializes in blood-derived products, Advanced Therapy Medicinal Products (ATMPs), and orphan drugs, with over 15 years of focused experience in navigating complex regulatory pathways.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • Processing hospital orders until 4 p.m. for same-day shipping with delivery before noon the next day
+1 more record
Product overview1 text field

Cevidra is an independent French pharmaceutical services company offering integrated continuum services for medicinal products to access the French market. The company operates as an Exploitant (marketing authorization holder representative) and provides a unified portfolio of services including Early Access Programs (EAP), Compassionate Use Programs, Market Access, Post-Market Surveillance, Supply Chain Optimization, Promotion & Sales, and Regulatory Compliance. Cevidra specializes in high value-added drugs for hospital use, with particular expertise in blood-derived products, ATMPs (Advanced Therapy Medicinal Products), and orphan drugs for rare diseases. The company also offers Tender Management services for the French public hospital procurement system.

Product and service5 records
1Exploitant status services for hospital pharmaceuticals
CategoryRegulatory services
Description

Provision of Cevidra's French Exploitant regulatory status to pharmaceutical manufacturers seeking to market high-value hospital drugs in France. This service enables clients to commercialize hospital pharmaceuticals without holding the Exploitant license themselves.

2Early access program (ATU) management
CategoryRegulatory services
Description

Regulatory and operational support for Authorization for Temporary Use (ATU) early access programs in France, enabling pharmaceutical companies to provide hospital drugs to patients before full market authorization.

3ATMP commercialization services
CategoryRegulatory services
Description

Regulatory pathway navigation and operational support for Advanced Therapy Medicinal Products (ATMPs) intended for the French hospital market.

4Orphan drug market access services
CategoryMarket access services
Description

End-to-end regulatory and market access support for orphan drugs targeting the French hospital market, leveraging Cevidra's specialized expertise in rare disease therapies.

5Blood-derived product regulatory services
CategoryRegulatory services
Description

Specialized regulatory and compliance services for blood-derived pharmaceuticals marketed through French hospitals.

Scale indicator2 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierMinorTypeOthers
Description

MabDesign is a biotherapy expert organization. Cevidra's partnership provides networking and visibility within the biotherapy and advanced therapy medicinal products ecosystem in France.

Strategic tierMinorTypeOthers
Description

Eurobiomed is a health innovation cluster. Cevidra's membership supports networking with other healthcare innovators and stakeholders in the Mediterranean region.

Strategic tierMinorTypeOthers
Description

EUCOPE represents pharmaceutical entrepreneurs at the European level. Cevidra's membership provides advocacy representation and regulatory intelligence at the EU level.

4AMLIS
Strategic tierMinorTypeOthers
Description

AMLIS is an organization supporting French SMEs for health. Cevidra's membership provides access to resources and support for small and medium-sized enterprises in the health sector.

cevidra.com
Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

France-based regulatory and market access consultancy serving pharma and biotech with EU/French HTA, clinical development, and pharmacovigilance support — directly comparable to Cevidra's regulatory + market access + pharmacovigilance stack for the French hospital market.

TypeDirect peer
Description

European regulatory affairs, market access and pharmacovigilance services firm comparable to Cevidra's Exploitant-style role, serving pharma/biotech sponsors seeking to commercialize in major EU markets including France.

TypeDirect peer
Description

Specialized pharmacovigilance and post-market surveillance service provider for pharma and biotech — directly comparable to Cevidra's Post-Market Surveillance and medical information offerings for the French market.

TypeDirect peer
Description

French-headquartered CRO and clinical/pharmaceutical services firm supporting biotech and pharma across regulatory and clinical operations — comparable as a France-anchored pharma services specialist competing in overlapping regulatory and market access work.

TypeRegional player
Description

France-based CRO offering regulatory, clinical, and product development services to pharma and crop science clients — comparable in French pharma regulatory services scope, though with a different vertical mix.

TypeBroad incumbent
Description

Global life sciences services leader spanning clinical, real-world evidence, regulatory, market access, and commercial services in France and globally — a broad incumbent whose market access and commercial offerings overlap with Cevidra's promotion & sales and market access services.

TypeBroad incumbent
Description

Global CRO with a sizeable market access, regulatory and pharmacovigilance practice across Europe — comparable as a broad incumbent competing for the same pharma/biotech regulatory and lifecycle management budgets that Cevidra targets in France.

TypeBroad incumbent
Description

Global clinical and commercial pharma services firm with regulatory, market access, and pharmacovigilance offerings — comparable in the commercial services overlay that competes with Cevidra's promotion & sales work for French launches.

TypeBroad incumbent
Description

Global CDMO and pharma services provider with development, manufacturing, and commercial supply capabilities in Europe — a broad incumbent whose secondary packaging, batch release, and distribution services overlap directly with Cevidra's supply chain optimization stack.

TypeBroad incumbent
Description

European-headquartered lab services and pharma services group with product testing, regulatory, and distribution-adjacent offerings — a broad incumbent operating across the pharma value chain with comparable reach into French pharmaceutical clients.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers2 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 profile1 record

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
Profiles1 record

Each record includes

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

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 →

Cevidra

Pharmaceutical Regulatory Servicescevidra.com

Cevidra is a French pharmaceutical services firm that acts as a regulated Exploitant, providing early access, market access, supply chain, and post-market surveillance services for high-value hospital drugs, including ATMPs, orphan drugs, and blood-derived products, primarily serving international and domestic pharma manufacturers entering the French hospital market.

What Cevidra does

Cevidra is a privately-held French pharmaceutical services firm headquartered in Grasse, France, founded in 2006 and operating with 11–50 employees under founder-CEO Stephane Destaing. The company operates as an Exploitant, a regulated status that legally allows it to market and distribute medicinal products in France on behalf of Marketing Authorization Holders not established in France. It provides an integrated continuum of pharmaceutical services — Early Access Programs, Compassionate Use / Named Patient Programs, Market Access, Post-Market Surveillance, Supply Chain Optimization, Promotion & Sales, and Regulatory Compliance — targeted at international and domestic pharmaceutical, biotech, ATMP, blood-product, and orphan-drug developers seeking entry into the French hospital market.

Cevidra's offerings are specialized around high-value, regulated therapeutic categories: blood-derived products, Advanced Therapy Medicinal Products (cell and gene therapies), and orphan drugs for rare diseases. Operationally, the firm maintains direct relationships with major French public hospital purchasing platforms (including RESPAN and UNIHA), responds to public tenders for hospital procurement, runs a 24/7 distribution operation with same-day shipping for orders placed before 4 p.m. and next-day delivery, and provides secondary packaging and batch release services. Pharmacist-led teams handle quality complaints, medical information requests, pharmacovigilance, and post-market surveillance. Industry association memberships (MabDesign, Eurobiomed, EUCOPE, AMLIS) embed Cevidra in the French and European biotherapy and SME health ecosystems.

Cevidra is a B2B professional-services business with quote-based, scope-dependent pricing; revenue mechanics are not publicly disclosed. The firm generates revenue across multiple customer segments — pharmaceutical manufacturers, biotech firms, ATMP developers, orphan-drug manufacturers, and blood-product companies — but is geographically concentrated entirely in France (Europe). There are no disclosed funding rounds, no parent company, and no indications of external private equity or venture capital backing; Cevidra appears to be an independent, founder/management-owned private company.

Cevidra firmographics

Firmographics
Name
Cevidra
Legal name
Cevidra
Website
https://cevidra.com
Company type
Private
Founded year
2006
Operating status
Operating
Headcount range
11–50 employees
Short description
Cevidra is a French pharmaceutical services firm that acts as a regulated Exploitant, providing early access, market access, supply chain, and post-market surveillance services for high-value hospital drugs, including ATMPs, orphan drugs, and blood-derived products, primarily serving international and domestic pharma manufacturers entering the French hospital market.
Ownership category
akta.pro rank

Where Cevidra is headquartered

Location

Headquarters

HQ city
Grasse
HQ country
France
HQ region
Europe

Offices2 records

Markets served

Cevidra business model

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

Revenue model

  1. Pharmaceutical Services: Cevidra generates revenue through comprehensive pharmaceutical services including early access programs, compassionate use programs, market access consulting, regulatory compliance, supply chain optimization, and promotion & sales services for medicinal products targeting the French hospital market.

Go-to-market motion2 records

Distribution channels3 records

Marketing channels3 records

Cevidra product offering

Product offering

Core offering

Cevidra is a French pharmaceutical services company founded in 2006 and based in Grasse, France. The company provides regulatory and operational support for marketing high-value drugs intended for hospital use in France, holding the Exploitant status required by French authorities. Cevidra specializes in blood-derived products, Advanced Therapy Medicinal Products (ATMPs), and orphan drugs, with over 15 years of focused experience in navigating complex regulatory pathways.

Product overview

Cevidra is an independent French pharmaceutical services company offering integrated continuum services for medicinal products to access the French market. The company operates as an Exploitant (marketing authorization holder representative) and provides a unified portfolio of services including Early Access Programs (EAP), Compassionate Use Programs, Market Access, Post-Market Surveillance, Supply Chain Optimization, Promotion & Sales, and Regulatory Compliance. Cevidra specializes in high value-added drugs for hospital use, with particular expertise in blood-derived products, ATMPs (Advanced Therapy Medicinal Products), and orphan drugs for rare diseases. The company also offers Tender Management services for the French public hospital procurement system.

Differentiator

Problem solved

Functional benefit

Products and services

  • Exploitant status services for hospital pharmaceuticals Provision of Cevidra's French Exploitant regulatory status to pharmaceutical manufacturers seeking to market high-value hospital drugs in France. This service enables clients to commercialize hospital pharmaceuticals without holding the Exploitant license themselves.
  • Early access program (ATU) management Regulatory and operational support for Authorization for Temporary Use (ATU) early access programs in France, enabling pharmaceutical companies to provide hospital drugs to patients before full market authorization.
  • ATMP commercialization services Regulatory pathway navigation and operational support for Advanced Therapy Medicinal Products (ATMPs) intended for the French hospital market.
  • Orphan drug market access services End-to-end regulatory and market access support for orphan drugs targeting the French hospital market, leveraging Cevidra's specialized expertise in rare disease therapies.
  • Blood-derived product regulatory services Specialized regulatory and compliance services for blood-derived pharmaceuticals marketed through French hospitals.

Quantifiable outcome

  • Processing hospital orders until 4 p.m. for same-day shipping with delivery before noon the next day
  • +1 more outcomes

Companies that use Cevidra

Customer profile

Named customers2 records

Segments4 records

Ideal customer profiles1 record

Cevidra technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Cevidra partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered minor.

  • MabDesignminorOthersMabDesign is a biotherapy expert organization. Cevidra's partnership provides networking and visibility within the biotherapy and advanced therapy medicinal products ecosystem in France.
  • EurobiomedminorOthersEurobiomed is a health innovation cluster. Cevidra's membership supports networking with other healthcare innovators and stakeholders in the Mediterranean region.
  • EUCOPE (European Confederation of Pharmaceutical Entrepreneurs AISBL)minorOthersEUCOPE represents pharmaceutical entrepreneurs at the European level. Cevidra's membership provides advocacy representation and regulatory intelligence at the EU level.
  • AMLISminorOthersAMLIS is an organization supporting French SMEs for health. Cevidra's membership provides access to resources and support for small and medium-sized enterprises in the health sector.

Scale indicators2 records

Recent moves6 records

Expansion highlights5 records

Cevidra competitors and assessment

Company assessment

Direct peers

  • Voisin Consulting Life Sciences: France-based regulatory and market access consultancy serving pharma and biotech with EU/French HTA, clinical development, and pharmacovigilance support — directly comparable to Cevidra's regulatory + market access + pharmacovigilance stack for the French hospital market.
  • PharmaLex (now part of Cencora/World Courier): European regulatory affairs, market access and pharmacovigilance services firm comparable to Cevidra's Exploitant-style role, serving pharma/biotech sponsors seeking to commercialize in major EU markets including France.
  • PrimeVigilance: Specialized pharmacovigilance and post-market surveillance service provider for pharma and biotech — directly comparable to Cevidra's Post-Market Surveillance and medical information offerings for the French market.
  • Aixial Group: French-headquartered CRO and clinical/pharmaceutical services firm supporting biotech and pharma across regulatory and clinical operations — comparable as a France-anchored pharma services specialist competing in overlapping regulatory and market access work.

Regional players

  • Staphyt: France-based CRO offering regulatory, clinical, and product development services to pharma and crop science clients — comparable in French pharma regulatory services scope, though with a different vertical mix.

Broad incumbents

  • IQVIA: Global life sciences services leader spanning clinical, real-world evidence, regulatory, market access, and commercial services in France and globally — a broad incumbent whose market access and commercial offerings overlap with Cevidra's promotion & sales and market access services.
  • ICON plc: Global CRO with a sizeable market access, regulatory and pharmacovigilance practice across Europe — comparable as a broad incumbent competing for the same pharma/biotech regulatory and lifecycle management budgets that Cevidra targets in France.
  • Syneos Health: Global clinical and commercial pharma services firm with regulatory, market access, and pharmacovigilance offerings — comparable in the commercial services overlay that competes with Cevidra's promotion & sales work for French launches.
  • Catalent: Global CDMO and pharma services provider with development, manufacturing, and commercial supply capabilities in Europe — a broad incumbent whose secondary packaging, batch release, and distribution services overlap directly with Cevidra's supply chain optimization stack.
  • Eurofins Scientific: European-headquartered lab services and pharma services group with product testing, regulatory, and distribution-adjacent offerings — a broad incumbent operating across the pharma value chain with comparable reach into French pharmaceutical clients.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Cevidra financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Cevidra leadership team

Management profile

Number of profiles

Profiles1 record

Cevidra funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Cevidra 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 Cevidra

What does Cevidra do?

Cevidra is a French pharmaceutical services company founded in 2006 and based in Grasse, France. The company provides regulatory and operational support for marketing high-value drugs intended for hospital use in France, holding the Exploitant status required by French authorities. Cevidra specializes in blood-derived products, Advanced Therapy Medicinal Products (ATMPs), and orphan drugs, with over 15 years of focused experience in navigating complex regulatory pathways.

Is Cevidra a public or private company?

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

When was Cevidra founded?

Cevidra was founded in 2006. It employs 11 to 50 people.

Where is Cevidra based?

Cevidra is headquartered in Grasse, France, in the Europe region.

How does Cevidra make money?

One revenue line is on record: pharmaceutical Services.

Who are Cevidra's main competitors?

Direct peers on record are Voisin Consulting Life Sciences, PharmaLex (now part of Cencora/World Courier), PrimeVigilance and Aixial Group. Staphyt is listed as a regional player. Broad incumbents are IQVIA, ICON plc, Syneos Health, Catalent and Eurofins Scientific.

Does Cevidra have an API?

No public API is recorded for Cevidra.

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