Roowin
Roowin is a French CRO founded in 1997 providing integrated fine chemistry, custom synthesis, cGMP API manufacturing, and analytical/stability services to pharmaceutical, biotechnology, fine chemicals, and cosmetics clients.
- Company typePrivate
- Founded1997
- HeadquartersRiom, France
- Headcount11–50
- GTM typeB2B
- OfferingServices
What Roowin does
Roowin is a privately held French Contract Research Organisation (CRO) founded in 1997 and headquartered in Riom (Auvergne region). The company provides an integrated suite of fine chemistry and cGMP API manufacturing services spanning five core practice areas: drug discovery, custom synthesis (50 mg to multi-kilogram scale), GMP synthesis, analytical chemistry, and ICH-compliant stress/stability studies. Operations are delivered across over 1,600 m² of facilities containing R&D laboratories, a cGMP kilolaboratory, and a pilot plant equipped with specialised reactors (photochemistry, high-pressure hydrogenation, microwave, peptide synthesis), Novasep preparative chromatography, and an extensive analytical instrumentation platform (NMR 300/500 MHz, GC/MS, UPLC/MS, HPLC, ICP-AES, DSC, TGA, FTIR).
The company generates revenue through project-based, fee-for-service engagements under a professional services model, with quotes delivered within 24-48 hours. Its primary customers are pharmaceutical and biotechnology firms requiring chemistry support from early discovery through clinical-phase API manufacturing, with secondary exposure to fine chemicals and cosmetics. Notable disclosed clients include Sanofi, Genfit, Wittycell, Sirona Biochem, and Pfa brei. Roowin has been cGMP compliant since 2007, holds ISO 9001 certification (since 2006), and is regularly inspected and approved by ANSM (most recently in September 2025). It has also advanced more than 100 molecules to clinic and claims to have supported first-batch production for startups now valued at billions.
The go-to-market is sales-led, leveraging direct expert consultation, industry conferences (e.g., BIOFIT 2023, AFSSI Connections), and dedicated international business development trips into the USA (since 2014) and Japan (since 2015). The company is recognised by the French government as a research undertaking, allowing eligible partners to recover 30% of project costs through the research subsidy programme — a structural cost advantage that supports pricing competitiveness.
Roowin firmographics
Firmographics- Name
- Roowin
- Legal name
- ROOWIN S.A.
- Website
- https://roowin.com
- Company type
- Private
- Founded year
- 1997
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Roowin is a French CRO founded in 1997 providing integrated fine chemistry, custom synthesis, cGMP API manufacturing, and analytical/stability services to pharmaceutical, biotechnology, fine chemicals, and cosmetics clients.
- Ownership category
- akta.pro rank
Roowin industry classification
Industry- Product category
- Pharmaceutical Contract Research & Manufacturing Services (CRO/CDMO)
- NAICS
- Scientific Research and Development Services (5417)
- SIC
- Services-Commercial Physical & Biological Research (8731)
- akta.pro primary industry
- Preclinical CROs (Discovery/Pharmacology/DMPK) (HLAGAAAB)
- akta.pro secondary industries
- Central Laboratory & Clinical Trial Testing CROs (HLAGAAAE), Toxicology & Safety Assessment CROs (GLP) (HLAGAAAC)
Keywords
Where Roowin is headquartered
LocationHeadquarters
- HQ city
- Riom
- HQ country
- France
- HQ region
- Europe
Offices2 records
Markets served
Roowin business model
Business model- GTM type
- B2B
- Offering type
- Services
- Cost components
- Personnel, Technology or R&D, Infrastructure, Operations, Marketing or Sales, Supply Chain
Revenue model
- Contract Research Services (CRO): Roowin operates as a CRO providing fee-for-service project-based engagements across drug discovery, custom synthesis, GMP API manufacturing, and analytical chemistry. Projects are scoped per client needs with no subscription model; revenue is earned on a per-project basis spanning from early discovery through clinical phase manufacturing.
- cGMP API Synthesis and Manufacturing: Production of Active Pharmaceutical Ingredients under cGMP conditions, ranging from 50 mg to several dozen kilograms, supporting exploratory stage through advanced clinical phases. Documentation, batch release, and regulatory compliance services are bundled into the manufacturing engagement.
- Stability and Analytical Testing Services: Forced degradation studies, stability studies under ICH guidelines, and analytical method development and validation services. Charged on a per-study or per-project basis.
Pricing tiers
| Model | Billing | Price |
|---|---|---|
| Other | Multi-year contract | Project-based pricing — custom quotes per engagement |
Go-to-market motion3 records
Distribution channels1 record
Marketing channels5 records
Roowin product offering
Product offeringCore offering
Roowin is a privately held French Contract Research Organisation (CRO) that delivers specialised fine chemistry services to the pharmaceutical, biotechnology, fine chemical, and cosmetics industries. The company operates over 1,600 m² of facilities in Riom (Auvergne, France), providing five integrated service lines — Drug Discovery, Custom Synthesis, GMP Synthesis, Analytical Chemistry, and Stress/Stability Studies — covering processes from medicinal chemistry through cGMP-compliant API production at scales from 50 mg to several dozen kilograms and supporting clients from IND/IMPD enabling work through advanced clinical phases.
Product overview
Roowin is a Contract Research Organisation (CRO) providing specialized fine chemistry services for the pharmaceutical and biotechnology industries. The company offers an integrated suite of five interconnected service lines: Drug Discovery Services (medicinal chemistry and early-stage research), Custom Synthesis Services (from milligram to multi-kilogram scale), GMP Synthesis Services (cGMP-compliant API production for clinical phases), Analytical Chemistry Services (comprehensive chemical analysis and method validation), and Stress/Stability Studies (ICH-compliant stability and degradation testing). These services are designed to support clients from early drug discovery through advanced clinical phases and small-scale commercial production, with capabilities spanning research laboratories, kilolaboratories, and pilot plant facilities totaling over 1600m².
Differentiator
Problem solved
Functional benefit
Products and services
- Drug Discovery Services Medicinal chemistry and early-stage drug discovery research services including lead optimization, synthesis of advanced intermediates, and support for research contracts from early discovery through preclinical phases. Targeted at pharmaceutical and biotech R&D teams needing medicinal chemistry expertise.
- Custom Synthesis Services Organic synthesis services ranging from 50 mg (medicinal chemistry scale) to several dozen kilograms, including process development, optimisation, and scale-up with capabilities such as hydrogenation, bromination, nitration, Curtius reaction, chiral chemistry, photochemistry, and cytotoxic reactions. Targeted at pharma, biotech, fine chemical, and cosmetics clients needing bespoke synthesis at multiple scales.
- GMP Synthesis Services cGMP-compliant API synthesis production supporting development from exploratory stage to advanced clinical phases (Phase I and beyond), with batch sizes from 50 mg to several dozen kilograms, complete production documentation, and regulatory compliance support for IND/IMPD submissions. Targeted at pharma and biotech clients running clinical-stage API manufacturing programs.
- Analytical Chemistry Services Comprehensive chemical analysis and separation services including method development and validation, chiral and non-chiral separations, ICH-compliant testing, with facilities equipped with NMR (300 MHz and 500 MHz), GC systems, UPLC/MS, HPLC units, ionic chromatography, DSC, TGA, FTIR, and ICP-AES. Targeted at pharma and biotech clients needing analytical method development, validation, and ICH-compliant testing.
- Stress / Stability Studies Forced degradation and stability studies following ICH guidelines, including accelerated degradation testing (oxidative, pH, temperature, humidity, photostress), with 8 stability chambers maintaining controlled conditions from -20°C to 40°C and 5–75% relative humidity. Targeted at pharma and biotech clients requiring ICH-compliant stability and forced degradation data for regulatory submissions.
Quantifiable outcome
- 100+ molecules advanced to clinic; first batches produced for dozens of startups, some now billion-dollar stock market valuations
- +3 more outcomes
Companies that use Roowin
Customer profileNamed customers5 records
Segments4 records
Ideal customer profiles3 records
Roowin technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature5 records
Roowin partnerships and signals
Strategic signalPartnerships
Six partnerships are on record, tiered notable, minor and core.
- Sirona BiochemnotableRoowin successfully completed the scale-up of Skin Lightening Compound SBM-TFC-1067 for Sirona Biochem, a Vancouver (British Columbia) based public company listed on TSX-V (SBM), Frankfurt (ZSB), and Xetra (ZSB.DE). This represents a direct client partnership for custom synthesis and scale-up services.
- SanofinotableSanofi is listed as a partner and client of Roowin, representing one of the major pharmaceutical companies served by the company's CRO/CDMO services.
- GenfitnotableGenfit is listed as a partner and client, representing Roowin's service relationship with a biotechnology company in the drug development sector.
- WittycellminorWittycell is listed as a partner and client of Roowin in the biotechnology sector.
- Pfa breiminorPfa brei is listed as a partner and client of Roowin in the cosmetics industry, representing the company's reach beyond pharmaceuticals into the cosmetics sector.
- French Government (Research Subsidy Programme)coreRoowin is recognised by the French government as a research undertaking organisation (organisme de recherche). Under this status, partners engaging Roowin for research projects can claim back 30% of project costs from the French government. Research expenses can be recovered at the end of the fiscal year, and special rates are available for companies not having benefited in the last 5 years.
Scale indicators10 records
Recent moves16 records
Roowin competitors and assessment
Company assessmentDirect peers
- Selvita: Polish contract research provider offering medicinal chemistry, custom synthesis, and analytical services. Comparable to Roowin in discovery chemistry and custom synthesis for early-stage biotech, with a similar European-mid-size positioning.
- Aenova: European CDMO offering API development, manufacturing, and analytical services to pharma and biotech. Direct peer in process chemistry and cGMP manufacturing, though typically operating at larger commercial scale than Roowin.
- Novasep: French CDMO providing API synthesis, custom manufacturing, and purification services including preparative chromatography. Comparable to Roowin in cGMP API manufacturing, complex process chemistry, and chromatography-based separations, with a stronger commercial-scale footprint.
- Hovione: Portuguese-headquartered specialty CDMO offering integrated API development, cGMP manufacturing, and particle engineering services to pharma and biotech. Directly comparable to Roowin in process chemistry, GMP API synthesis, and analytical services for clinical-phase supply.
- ChemPartner: China-headquartered CRO/CDMO providing medicinal chemistry, process chemistry, and cGMP API manufacturing for global pharma and biotech. Comparable in integrated discovery-to-GMP model and target client base (emerging biotech), with significantly larger headcount.
- PCI Synthesis: US-based CDMO offering custom API development, cGMP manufacturing, and process chemistry for early- to mid-stage pharma and biotech. Comparable to Roowin in clinical-phase API supply and integrated analytical services.
- Carbogen Amcis: Swiss-based CDMO specialising in API development, process chemistry, and cGMP manufacturing from clinical to commercial scale. Overlaps directly with Roowin's custom synthesis, GMP synthesis, and analytical chemistry offerings for pharma/biotech clients.
Broad incumbents
- Almac Group: Northern Ireland-headquartered CDMO providing API development, analytical services, and cGMP manufacturing for pharma. Overlaps with Roowin in analytical chemistry and clinical-phase API supply, but at significantly larger scale and broader service portfolio.
- Eurofins Discovery: Large European contract research services provider offering drug discovery, medicinal chemistry, and in vitro pharmacology services. Overlaps with Roowin's drug discovery and custom synthesis offerings, but at significantly greater scale and breadth.
- Evotec (including former Aptuit): Global CRO/CDMO offering integrated drug discovery, CMC, and API manufacturing services. Comparable in integrated discovery-to-GMP positioning but operates at much larger scale and broader service portfolio than Roowin.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat6 records
Key risks6 records
Key highlights7 records
Customer concentration
Roowin social profiles
Digital presenceRoowin compliance and trust
Trust signalCompliance6 records
Roowin financial estimates
Financial estimateRevenue estimate
Valuation estimate
Roowin leadership team
Management profileNumber of profiles
Profiles5 records
Roowin funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Roowin M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Roowin
What does Roowin do?
Roowin is a privately held French Contract Research Organisation (CRO) that delivers specialised fine chemistry services to the pharmaceutical, biotechnology, fine chemical, and cosmetics industries. The company operates over 1,600 m² of facilities in Riom (Auvergne, France), providing five integrated service lines — Drug Discovery, Custom Synthesis, GMP Synthesis, Analytical Chemistry, and Stress/Stability Studies — covering processes from medicinal chemistry through cGMP-compliant API production at scales from 50 mg to several dozen kilograms and supporting clients from IND/IMPD enabling work through advanced clinical phases.
Is Roowin a public or private company?
Roowin is a private company. It is classified as founder individual operated bootstrapped and is currently operating.
When was Roowin founded?
Roowin was founded in 1997. It employs 11 to 50 people.
Where is Roowin based?
Roowin is headquartered in Riom, France, in the Europe region.
How does Roowin make money?
Three revenue lines are on record. Contract Research Services (CRO) is the primary driver. The others are cGMP API Synthesis and Manufacturing and stability and Analytical Testing Services.
Who are Roowin's main competitors?
Direct peers on record are Selvita, Aenova, Novasep, Hovione, ChemPartner, PCI Synthesis and Carbogen Amcis. Broad incumbents are Almac Group, Eurofins Discovery and Evotec (including former Aptuit).
Does Roowin have an API?
No public API is recorded for Roowin.
What industry is Roowin in?
Roowin's product category is Pharmaceutical Contract Research & Manufacturing Services (CRO/CDMO). Its primary akta.pro industry code is HLAGAAAB, Preclinical CROs (Discovery/Pharmacology/DMPK), with a secondary code of HLAGAAAE, Central Laboratory & Clinical Trial Testing CROs. Its NAICS code is 5417 and its SIC code is 8731.