Developer docs
API playgroundTry for free, no card

Search company profiles

SkyePharma

Full company profile

uuid003bnvs

Namestring
SkyePharma
Legal namestring
Skyepharma Production S.A.S.
Company typeenum
Private
Founded yearint
1996
Descriptiontext

Skyepharma Production S.A.S. is a privately held French Contract Development and Manufacturing Organization (CDMO) specializing in complex oral solid dosage forms — tablets, capsules, granules, pellets, and stick-packs. Headquartered in Saint-Quentin-Fallavier (Auvergne-Rhône-Alpes), the company operates from a single integrated cGMP-certified site with multi-regulatory approvals (FDA, ANSM, ANVISA, BPF) that enable supply into more than 160 countries. It employs 217 people, roughly a quarter of whom hold PhDs in chemistry or pharmaceutical sciences. Skyepharma's customer base spans large pharmaceutical companies (Bayer, Teva, Dr. Reddy's, Chiesi, Azurity, Therabel, Advanz), specialty pharma (Bioprojet, Pharmadev), and biotechs (MaaT Pharma, Biophytis, Calliditas), addressing formulation challenges including poor bioavailability, controlled/targeted release, multi-API combinations, HPAPI containment, and small-volume orphan drug production.

The company's competitive differentiation rests on three proprietary patented drug-delivery platforms: Geomatrix® (multi-layer controlled-release tablets, present in 8 commercial products across 80+ countries), Geoclock® (tab-in-tab technology enabling time-programmed release independent of food or pH), and Soctec® (gastro-retentive capsules designed to remain in the stomach for over 9 hours). It also operates four forward-looking R&D programs — GeoBiologicS (oral biologics delivery with University of Bordeaux), NanoMicS/NanoFact (nanoparticle formulations, University of Lyon), GeoColon (colon targeting, University of Lille), and MucoTabS (mucoadhesive platforms, University of Lyon) — plus specialized contained production zones for OEB 4/5 highly potent molecules (450 m², opened November 2024), non-sexual hormones (~1,000 m²), and microbiome therapies (Skyehub-Bioproduction, 1,600+ m², co-developed with MaaT Pharma).

Skyepharma generates revenue across five streams: (1) galenic formulation development services from preclinical through Phase III using Quality by Design methodology; (2) cGMP manufacturing of clinical and commercial oral solid doses; (3) primary and secondary packaging including serialization for multi-market compliance; (4) Skyehub-Bioproduction modular GMP infrastructure offered to biotech clients; and (5) licensing royalties from Geomatrix® and Geoclock®. Pricing is project-based and not publicly disclosed. The go-to-market is direct B2B enterprise sales, with prospecting, RFP management, and commercial negotiation handled by an in-house business development team targeting EU and US markets, supported by participation in industry events such as CDMO Live, CPHI, BayOconnect, and the Orphan Drug Congress.

Short descriptiontext

Skyepharma is a French CDMO specializing in complex oral solid dosage forms (tablets, capsules, pellets) for pharmaceutical and biotech clients, leveraging proprietary controlled-release platforms (Geomatrix®, Geoclock®, Soctec®) and specialized HPAPI, hormone, and bioproduction facilities certified by FDA, ANSM, and ANVISA.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersSaint-quentin-fallavier, France
HQ citystring
Saint-quentin-fallavier
HQ countrystring
France
HQ regionstring
Europe
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
pharmaceutical CDMO services, oral solid dosage manufacturing, controlled-release drug delivery, pharmaceutical formulation development, cGMP contract manufacturing
Industry2 codes
1CMC & Pharmaceutical Development (Formulation/Process/Analytical Development)
CodeHLAIALADPrimaryYes
2Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC)
CodeHLAGAHAMPrimaryNo
NAICS code3 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Scientific Research and Development Services5417
  • Packaging and Labeling Services561910
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Pharmaceutical CDMO Services
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model5 records
1Pharmaceutical Development Services
TypeProfessional Services
Description

Galenic formulation development from early-stage through clinical phase I-III, including analytical development and Quality by Design methodology. Services span from proof of concept to regulatory dossier.

skyepharma.fr
2cGMP Manufacturing
TypeOne Time License
Description

Manufacturing of oral solid dosage forms including tablets (standard, multi-layer, coated), capsules, granules, and pellets. Covers clinical batches through commercial-scale industrial production, with flexible lot sizes.

skyepharma.fr
3Pharmaceutical Packaging
TypeOne Time License
Description

Primary and secondary packaging including bottles, blisters, stick-packs, with serialization and aggregation for international regulatory compliance (Europe, USA, Russia, Saudi Arabia).

skyepharma.fr
4Skyehub-Bioproduction
TypeManaged Services
Description

Dedicated GMP facilities and scientific/quality/production teams offered on a modular basis to biotech companies for clinical (phase 2-3) through industrialization. Includes building access, equipment installation, and turnkey manufacturing solutions.

skyepharma.fr
5Licensing of Proprietary Technologies
TypeLicensing Royalties
Description

Access to proprietary technologies Geomatrix® and Geoclock® through licensing arrangements for pharmaceutical partners developing controlled-release products.

skyepharma.fr
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components6 values
Personnel, Operations, Infrastructure, Technology or R&D, Marketing or Sales, Supply Chain
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 record
1Skyehub-Bioproduction
Description

A turnkey infrastructure solution offering dedicated GMP-certified facilities, quality systems, industrial support, and a qualified production team for biotech companies, from clinical phases through industrialization.

skyepharma.fr
Core offering1 text field

SkyePharma is a French pharmaceutical CDMO that develops, manufactures, and packages complex oral solid dosage forms (tablets, capsules, granules, pellets, stick-packs) for pharmaceutical and biotech clients. Its core offering is built around proprietary controlled-release technology platforms (Geomatrix®, Geoclock®, Soctec®) and includes galenic formulation development, cGMP manufacturing, packaging with serialization, project management, and modular bioproduction services (Skyehub-Bioproduction).

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • Geomatrix® technology used in 8 marketed products distributed in over 80 countries
+4 more records
Product overview1 text field

SkyePharma is a French Contract Development and Manufacturing Organization (CDMO) specializing in complex solid oral dosage forms, offering an integrated service portfolio from early-stage development through industrial manufacturing and packaging. The core offering centers on proprietary controlled-release technology platforms including Geomatrix® (multi-layer tablets), Geoclock® (programmed-release tab-in-tab technology), and Soctec® (gastro-retentive capsules). SkyePharma provides end-to-end CDMO services including galenic formulation development, pharmaceutical manufacturing of tablets/capsules/granules/stick-packs, packaging with serialization, and regulatory support. The company also operates specialized facilities for highly potent compounds (OEB 4/5), non-sexual hormones, and biopharmaceuticals through its Skyehub-Bioproduction platform. Additional innovation programs include GeoBiologicS (oral biologics delivery), NanoMicS/NanoFact (nanoparticle formulations), GeoColon (colon targeting), and MucoTabS (mucoadhesive platforms).

Product and service10 records
1Geomatrix® Multi-Layer Tablet Technology
CategoryProprietary Technology Platform (Licensing)
2Geoclock® Tab-in-Tab Programmed-Release Technology
CategoryProprietary Technology Platform (Licensing)
3Skyehub-Bioproduction Modular Bioproduction Service
CategoryBiopharmaceutical Manufacturing Service
4Galenic Formulation Development Services
CategoryPharmaceutical Development Service
5cGMP Pharmaceutical Manufacturing Service
CategoryContract Manufacturing Service
6Pharmaceutical Packaging Service
CategoryPharmaceutical Packaging Service
7Pharmaceutical Project Management Service
CategoryCDMO Project Management Service
8HPAPI Manufacturing (OEB 4/5) Service
CategorySpecialty Contract Manufacturing (HPAPI)
9Non-Sexual Hormones Manufacturing Service
CategorySpecialty Contract Manufacturing (Hormones)
10Multi-API Combination Formulation Service
CategorySpecialty Formulation Service
Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2022-02-01
Description

In February 2022, Skyepharma and MaaT Pharma established a partnership to create the first Skyehub building, a dedicated cGMP (BPF) manufacturing facility for microbiome ecosystem therapies in France. The facility spans over 1,600 m² and represents a unique co-development arrangement where Skyepharma provides turnkey GMP infrastructure, production teams, quality systems, and industrial resources while MaaT Pharma gains exclusive manufacturing capacity for its microbiome therapy products.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Portugal-based CDMO with proprietary particle engineering and controlled-release capabilities; comparable emphasis on complex formulation challenges and pharmaceutical innovation partnerships.

TypeDirect peer
Description

French-headquartered CDMO with broad dosage-form coverage including oral solids; comparable French-based contract manufacturing services to large pharma customers across Europe.

TypeDirect peer
Description

Global CDMO with deep specialty in oral solid dose forms and proprietary softgel/controlled-release technologies; directly comparable service portfolio and customer base to SkyePharma, but at vastly larger scale.

TypeEmerging player
Description

Canadian specialty CDMO focused on oral solid dose manufacturing including highly potent compounds; emerging peer with niche HPAPI/oral solids capability analogous to SkyePharma's HPAPI zone offering.

TypeDirect peer
Description

US-headquartered specialty CDMO built around proprietary oral drug delivery platforms (multiparticulate, taste masking, controlled release); the most direct comparable in terms of differentiated technology + CDMO service integration.

TypeDirect peer
Description

Swedish-origin CDMO with strong oral solids and inhalation capabilities; comparable European footprint, B2B pharma customer base, and contract development + commercial manufacturing model.

TypeDirect peer
Description

French CDMO with multiple European sites producing solid, sterile, and liquid dosage forms; geographically proximate peer serving the same French and European pharma customer base.

TypeDirect peer
Description

European-headquartered CDMO specializing in solid oral dosage forms (tablets, capsules, softgels) with multiple EU sites; closely comparable business model, customer base, and proprietary formulation focus.

TypeBroad incumbent
Description

Global CDMO leader with extensive oral solids, biologics, and cell/gene therapy capabilities; competes with SkyePharma for complex formulation projects but at much greater scale and broader modality coverage.

TypeBroad incumbent
Description

Pharmaceutical CDMO services arm of Eurofins Scientific offering development, manufacturing, and analytical services; broader portfolio but overlaps on formulation development and clinical/commercial supply.

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 customers12 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
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature7 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles5 records

Each record includes

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

No data
Compliance5 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&A1 record

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 →

SkyePharma

Pharmaceutical CDMO Servicesskyepharma.fr

Skyepharma is a French CDMO specializing in complex oral solid dosage forms (tablets, capsules, pellets) for pharmaceutical and biotech clients, leveraging proprietary controlled-release platforms (Geomatrix®, Geoclock®, Soctec®) and specialized HPAPI, hormone, and bioproduction facilities certified by FDA, ANSM, and ANVISA.

What SkyePharma does

Skyepharma Production S.A.S. is a privately held French Contract Development and Manufacturing Organization (CDMO) specializing in complex oral solid dosage forms — tablets, capsules, granules, pellets, and stick-packs. Headquartered in Saint-Quentin-Fallavier (Auvergne-Rhône-Alpes), the company operates from a single integrated cGMP-certified site with multi-regulatory approvals (FDA, ANSM, ANVISA, BPF) that enable supply into more than 160 countries. It employs 217 people, roughly a quarter of whom hold PhDs in chemistry or pharmaceutical sciences. Skyepharma's customer base spans large pharmaceutical companies (Bayer, Teva, Dr. Reddy's, Chiesi, Azurity, Therabel, Advanz), specialty pharma (Bioprojet, Pharmadev), and biotechs (MaaT Pharma, Biophytis, Calliditas), addressing formulation challenges including poor bioavailability, controlled/targeted release, multi-API combinations, HPAPI containment, and small-volume orphan drug production.

The company's competitive differentiation rests on three proprietary patented drug-delivery platforms: Geomatrix® (multi-layer controlled-release tablets, present in 8 commercial products across 80+ countries), Geoclock® (tab-in-tab technology enabling time-programmed release independent of food or pH), and Soctec® (gastro-retentive capsules designed to remain in the stomach for over 9 hours). It also operates four forward-looking R&D programs — GeoBiologicS (oral biologics delivery with University of Bordeaux), NanoMicS/NanoFact (nanoparticle formulations, University of Lyon), GeoColon (colon targeting, University of Lille), and MucoTabS (mucoadhesive platforms, University of Lyon) — plus specialized contained production zones for OEB 4/5 highly potent molecules (450 m², opened November 2024), non-sexual hormones (~1,000 m²), and microbiome therapies (Skyehub-Bioproduction, 1,600+ m², co-developed with MaaT Pharma).

Skyepharma generates revenue across five streams: (1) galenic formulation development services from preclinical through Phase III using Quality by Design methodology; (2) cGMP manufacturing of clinical and commercial oral solid doses; (3) primary and secondary packaging including serialization for multi-market compliance; (4) Skyehub-Bioproduction modular GMP infrastructure offered to biotech clients; and (5) licensing royalties from Geomatrix® and Geoclock®. Pricing is project-based and not publicly disclosed. The go-to-market is direct B2B enterprise sales, with prospecting, RFP management, and commercial negotiation handled by an in-house business development team targeting EU and US markets, supported by participation in industry events such as CDMO Live, CPHI, BayOconnect, and the Orphan Drug Congress.

SkyePharma firmographics

Firmographics
Name
SkyePharma
Legal name
Skyepharma Production S.A.S.
Website
https://www.skyepharma.fr/
Company type
Private
Founded year
1996
Operating status
Operating
Headcount range
101–250 employees
Short description
Skyepharma is a French CDMO specializing in complex oral solid dosage forms (tablets, capsules, pellets) for pharmaceutical and biotech clients, leveraging proprietary controlled-release platforms (Geomatrix®, Geoclock®, Soctec®) and specialized HPAPI, hormone, and bioproduction facilities certified by FDA, ANSM, and ANVISA.
Ownership category
akta.pro rank

SkyePharma industry classification

Industry
Product category
Pharmaceutical CDMO Services
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Scientific Research and Development Services (5417), Packaging and Labeling Services (561910)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
CMC & Pharmaceutical Development (Formulation/Process/Analytical Development) (HLAIALAD)
akta.pro secondary industry
Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC) (HLAGAHAM)

Keywords

  • Pharmaceutical CDMO services
  • Oral solid dosage manufacturing
  • Controlled-release drug delivery
  • Pharmaceutical formulation development
  • CGMP contract manufacturing

Where SkyePharma is headquartered

Location

Headquarters

HQ city
Saint-quentin-fallavier
HQ country
France
HQ region
Europe

Offices1 record

Markets served

SkyePharma business model

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

Revenue model

  1. Pharmaceutical Development Services: Galenic formulation development from early-stage through clinical phase I-III, including analytical development and Quality by Design methodology. Services span from proof of concept to regulatory dossier.
  2. cGMP Manufacturing: Manufacturing of oral solid dosage forms including tablets (standard, multi-layer, coated), capsules, granules, and pellets. Covers clinical batches through commercial-scale industrial production, with flexible lot sizes.
  3. Pharmaceutical Packaging: Primary and secondary packaging including bottles, blisters, stick-packs, with serialization and aggregation for international regulatory compliance (Europe, USA, Russia, Saudi Arabia).
  4. Skyehub-Bioproduction: Dedicated GMP facilities and scientific/quality/production teams offered on a modular basis to biotech companies for clinical (phase 2-3) through industrialization. Includes building access, equipment installation, and turnkey manufacturing solutions.
  5. Licensing of Proprietary Technologies: Access to proprietary technologies Geomatrix® and Geoclock® through licensing arrangements for pharmaceutical partners developing controlled-release products.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels5 records

SkyePharma product offering

Product offering

Core offering

SkyePharma is a French pharmaceutical CDMO that develops, manufactures, and packages complex oral solid dosage forms (tablets, capsules, granules, pellets, stick-packs) for pharmaceutical and biotech clients. Its core offering is built around proprietary controlled-release technology platforms (Geomatrix®, Geoclock®, Soctec®) and includes galenic formulation development, cGMP manufacturing, packaging with serialization, project management, and modular bioproduction services (Skyehub-Bioproduction).

Product overview

SkyePharma is a French Contract Development and Manufacturing Organization (CDMO) specializing in complex solid oral dosage forms, offering an integrated service portfolio from early-stage development through industrial manufacturing and packaging. The core offering centers on proprietary controlled-release technology platforms including Geomatrix® (multi-layer tablets), Geoclock® (programmed-release tab-in-tab technology), and Soctec® (gastro-retentive capsules). SkyePharma provides end-to-end CDMO services including galenic formulation development, pharmaceutical manufacturing of tablets/capsules/granules/stick-packs, packaging with serialization, and regulatory support. The company also operates specialized facilities for highly potent compounds (OEB 4/5), non-sexual hormones, and biopharmaceuticals through its Skyehub-Bioproduction platform. Additional innovation programs include GeoBiologicS (oral biologics delivery), NanoMicS/NanoFact (nanoparticle formulations), GeoColon (colon targeting), and MucoTabS (mucoadhesive platforms).

Differentiator

Problem solved

Functional benefit

Brands

  • Skyehub-Bioproduction: A turnkey infrastructure solution offering dedicated GMP-certified facilities, quality systems, industrial support, and a qualified production team for biotech companies, from clinical phases through industrialization.

Products and services

  • Geomatrix® Multi-Layer Tablet Technology
  • Geoclock® Tab-in-Tab Programmed-Release Technology
  • Skyehub-Bioproduction Modular Bioproduction Service
  • Galenic Formulation Development Services
  • cGMP Pharmaceutical Manufacturing Service
  • Pharmaceutical Packaging Service
  • Pharmaceutical Project Management Service
  • HPAPI Manufacturing (OEB 4/5) Service
  • Non-Sexual Hormones Manufacturing Service
  • Multi-API Combination Formulation Service

Quantifiable outcome

  • Geomatrix® technology used in 8 marketed products distributed in over 80 countries
  • +4 more outcomes

Companies that use SkyePharma

Customer profile

Named customers12 records

Segments4 records

Ideal customer profiles4 records

SkyePharma technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature7 records

SkyePharma partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • MaaT PharmacoreStrategic or Co-development Partner · 1 February 2022In February 2022, Skyepharma and MaaT Pharma established a partnership to create the first Skyehub building, a dedicated cGMP (BPF) manufacturing facility for microbiome ecosystem therapies in France. The facility spans over 1,600 m² and represents a unique co-development arrangement where Skyepharma provides turnkey GMP infrastructure, production teams, quality systems, and industrial resources while MaaT Pharma gains exclusive manufacturing capacity for its microbiome therapy products.

Scale indicators9 records

Recent moves6 records

Expansion highlights6 records

SkyePharma competitors and assessment

Company assessment

Direct peers

  • Hovione: Portugal-based CDMO with proprietary particle engineering and controlled-release capabilities; comparable emphasis on complex formulation challenges and pharmaceutical innovation partnerships.
  • Fareva: French-headquartered CDMO with broad dosage-form coverage including oral solids; comparable French-based contract manufacturing services to large pharma customers across Europe.
  • Catalent: Global CDMO with deep specialty in oral solid dose forms and proprietary softgel/controlled-release technologies; directly comparable service portfolio and customer base to SkyePharma, but at vastly larger scale.
  • Adare Pharma Solutions: US-headquartered specialty CDMO built around proprietary oral drug delivery platforms (multiparticulate, taste masking, controlled release); the most direct comparable in terms of differentiated technology + CDMO service integration.
  • Recipharm: Swedish-origin CDMO with strong oral solids and inhalation capabilities; comparable European footprint, B2B pharma customer base, and contract development + commercial manufacturing model.
  • Delpharm: French CDMO with multiple European sites producing solid, sterile, and liquid dosage forms; geographically proximate peer serving the same French and European pharma customer base.
  • Aenova: European-headquartered CDMO specializing in solid oral dosage forms (tablets, capsules, softgels) with multiple EU sites; closely comparable business model, customer base, and proprietary formulation focus.

Emerging players

  • Pillar5 Pharma: Canadian specialty CDMO focused on oral solid dose manufacturing including highly potent compounds; emerging peer with niche HPAPI/oral solids capability analogous to SkyePharma's HPAPI zone offering.

Broad incumbents

  • Lonza: Global CDMO leader with extensive oral solids, biologics, and cell/gene therapy capabilities; competes with SkyePharma for complex formulation projects but at much greater scale and broader modality coverage.
  • Eurofins CDMO: Pharmaceutical CDMO services arm of Eurofins Scientific offering development, manufacturing, and analytical services; broader portfolio but overlaps on formulation development and clinical/commercial supply.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

SkyePharma social profiles

Digital presence

SkyePharma compliance and trust

Trust signal

Compliance5 records

SkyePharma financial estimates

Financial estimate

Revenue estimate

Valuation estimate

SkyePharma leadership team

Management profile

Number of profiles

Profiles5 records

SkyePharma funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

SkyePharma M&A and investment

M&A and investment

M&A1 record

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about SkyePharma

What does SkyePharma do?

SkyePharma is a French pharmaceutical CDMO that develops, manufactures, and packages complex oral solid dosage forms (tablets, capsules, granules, pellets, stick-packs) for pharmaceutical and biotech clients. Its core offering is built around proprietary controlled-release technology platforms (Geomatrix®, Geoclock®, Soctec®) and includes galenic formulation development, cGMP manufacturing, packaging with serialization, project management, and modular bioproduction services (Skyehub-Bioproduction).

Is SkyePharma a public or private company?

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

When was SkyePharma founded?

SkyePharma was founded in 1996. It employs 101 to 250 people.

Where is SkyePharma based?

SkyePharma is headquartered in Saint-quentin-fallavier, France, in the Europe region.

How does SkyePharma make money?

Five revenue lines are on record. Pharmaceutical Development Services are the primary driver. The others are cGMP Manufacturing, pharmaceutical Packaging, skyehub-Bioproduction and licensing of Proprietary Technologies.

Who are SkyePharma's main competitors?

Direct peers on record are Hovione, Fareva, Catalent, Adare Pharma Solutions, Recipharm, Delpharm and Aenova. Pillar5 Pharma is listed as an emerging player. Broad incumbents are Lonza and Eurofins CDMO.

Does SkyePharma have an API?

No public API is recorded for SkyePharma.

What industry is SkyePharma in?

SkyePharma's product category is Pharmaceutical CDMO Services. Its primary akta.pro industry code is HLAIALAD, CMC & Pharmaceutical Development (Formulation/Process/Analytical Development), with a secondary code of HLAGAHAM, Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC). Its NAICS code is 541714 and its SIC code is 2834.

Unlock the full company data

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

Contact sales
Live signals
GlobeNewswireeureKING, the first European SPAC in healthcare dedicated to biomanufacturing, announces the signature of a put option for the potential acquisition of Skyepharma to build a new European bio-CDMO leadeureKING signed a put option to acquire Skyepharma, a French CDMO, for a €30.2 million cash purchase plus shares. The deal values Skyepharma at an enterprise value of circa €50 million and equity value of circa €52 million. The transaction is expected to close by August 31, 2023.GlobeNewswireeureKING, the first European SPAC in healthcare dedicated to biomanufacturing, announces its intention to combine with Skyepharma to build a new European bio-CDMO leadereureKING, a European SPAC, submitted a firm offer to acquire Skyepharma, a French CDMO, with an exclusivity period. The deal, expected to close in September 2023, would create a European bio-CDMO leader. Closing is subject to shareholder approval and regulatory conditions.GlobeNewswireSkyePharma PLC announces Final ResultsSkyePharma PLC reported 2009 results with revenue of GBP55.9m, down 10% from GBP62.2m, and a net loss of GBP1.4m after tax. Pre-exceptional operating profit rose 39% to GBP15.1m, and cash and undrawn facilities stood at GBP29.3m. The company expects 2010 revenues broadly in line with 2009.GlobeNewswireSkyepharma PLC announces - Regulatory UpdateSkyePharma PLC received a Complete Response Letter from the FDA on its Flutiform NDA for fluticasone/formoterol in persistent asthma, citing substantive issues requiring additional clinical work. The company will seek discussions with the FDA to determine next steps, with further impact details to be announced. Net cash as at 31 December 2009 was GBP27 million.GlobeNewswireSkyepharma PLC - Board ChangeSkyePharma PLC announced that Chairman Jeremy Scudamore will step down at the end of 2009 for health reasons. Frank Condella, Non-Executive Director, will take over as Chairman from 1 January 2010. CEO Ken Cunningham said Condella will bring continuity and deep business understanding.GlobeNewswireSkyepharma PLC - Interim Management StatementSkyePharma PLC published its interim management statement on November 12, 2009, reporting cash of GBP23.8 million as of June 30, 2009, plus GBP5.0 million received in July and GBP1.5 million in October. The company noted Flutiform's Phase III completion and FDA dosing data requirements, with US approval unlikely before 2012.GlobeNewswireSKYEPHARMA PLC - Research UpdateSkyePharma held a meeting with the FDA on its Flutiform NDA, confirming additional clinical work on dosing is required. The company expects US approval unlikely before the second half of 2011, while Europe and Japan remain on track. Abbott will fund trials and recoup costs from milestones.GlobeNewswireSkyepharma PLC announces Conversion of BondsSkyePharma PLC converted GBP2.5 million of its 6% 2024 convertible bonds into 673,854 ordinary shares at GBP3.71 per share. The conversion reduces debt by GBP6.587 million, saving GBP395,220 in annual interest and cutting finance costs by GBP150,000 per year.GlobeNewswireSkyepharma PLC Announces Research UpdateSkyePharma announced the FDA issued a 74-day letter on its Flutiform NDA, confirming the application is complete for substantive review. The FDA preliminarily noted potential review issues, likely requiring additional clinical work on dosing, which could extend the review timeline. The company is seeking discussions with the FDA to address these issues.GlobeNewswireSkyePharma PLC: Flutiform NDA Accepted for ReviewSkyePharma announced the FDA accepted its NDA for Flutiform, a fixed-dose asthma inhaler combining fluticasone and formoterol. The filing fee of $1.2 million will be deducted from a $2 million payment due. If approved, it would be the first such combination in the US.