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Selvita

Full company profile

uuid002jud6

Namestring
Selvita
Legal namestring
Selvita S.A.
Websiteurl
selvita.com
Company typeenum
Public
Founded yearint
2007
Descriptiontext

Selvita S.A. is a Poland-headquartered, publicly listed contract research organization (CRO) founded in 2007 and traded on the Warsaw Stock Exchange (WSE:SLV). Following a 2019 corporate split that separated proprietary oncology drug discovery into Ryvu Therapeutics, Selvita has operated as a pure-play CRO delivering integrated drug discovery and drug development services to pharmaceutical and biotechnology companies across Europe, North America, and Asia. The company employs more than 950 scientists across research facilities in Kraków, Poznań, and Wrocław (Poland) and Zagreb (Croatia), with commercial subsidiaries in Boston, San Francisco, and Cambridge UK, and serves smaller agrochemical clients through a GLP-compliant analytical testing arm.

The company's core offering is organized into three pillars: Drug Discovery (target validation through preclinical candidate nomination across small molecules, antibodies, and protein degraders), Drug Development (CMC analytical services, formulation, GMP manufacturing, stability studies, QP release, and regulatory affairs under GMP/GLP), and Contract Testing (GxP-compliant analytical services for pharma and agrochemical clients). Underlying the discovery pillar is an integrated technology stack that includes the proprietary TADAM deep-learning virtual screening model (processing 50M+ compounds per hour on NVIDIA H100 GPUs), structure-based drug design with advanced molecular dynamics, CADD/AI for ADMET and selectivity prediction, protein sciences (X-ray, cryo-EM, fragment-based discovery), high-content screening with computer vision, and a multi-omics hub covering genomics, transcriptomics, proteomics, and metabolomics. Recent platform additions include the CPSA cellular target engagement technology (launched November 2025) and a nanobody discovery partnership with Llamatech (June 2026).

Selvita monetizes via professional-services engagements delivered under full-time equivalent (FTE) or fee-for-service contracts of multi-year duration, with global regulatory compliance (FDA, EMA, ICH) and full IP retention by the client as standard terms. The company has scaled through a combination of organic expansion (Hexagon headquarters in Kraków 2023, Wrocław site 2024, US/UK subsidiaries from 2015-2016) and targeted M&A (BioCentrum 2008, Fidelta from Galapagos 2021, PozLab 2024), funded by a 2014 IPO (PLN 27.3M) and a 2020 secondary offering (EUR 20.6M). Most recently, Q1 2026 operating revenues were EUR 19.1M at a 14% EBITDA margin, with Drug Development growing 6% YoY while Drug Discovery declined against a softer European outsourced discovery market.

Short descriptiontext

Selvita is a Poland-headquartered, publicly listed CRO delivering integrated drug discovery, drug development, and GxP-compliant analytical services to pharmaceutical, biotechnology, and agrochemical clients worldwide.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1,001–5,000
akta.pro rankint
HeadquartersKraków, Poland
HQ citystring
Kraków
HQ countrystring
Poland
HQ regionstring
Europe
Markets served

Serves global market

Offices7 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
contract research services, drug discovery services, preclinical drug development, medicinal chemistry services, pharmaceutical R&D outsourcing
Industry4 codes
PRIMARYHLAGAAAB
Preclinical CROs (Discovery/Pharmacology/DMPK)
SECONDARYHLAGAAAC
Toxicology & Safety Assessment CROs (GLP)
SECONDARYHLAGAAAE
Central Laboratory & Clinical Trial Testing CROs
SECONDARYHLAGAOAE
Quality Assurance, GxP Compliance & Auditing FSP
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Scientific Staffing & Functional Service Providers (FSP)
NAICS code2 codes
  • Scientific Research and Development Services5417
  • Testing Laboratories and Services54138
SIC code2 codes
  • Services-Commercial Physical & Biological Research8731
  • Services-Testing Laboratories8734
Product category
Contract Research Organization (CRO) Services
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model4 records
1Drug Discovery Services
TypeProfessional Services
Description

Integrated or standalone solutions spanning medicinal chemistry, biology, DMPK, and protein sciences from target validation to preclinical candidate nomination. Delivered via FTE or fee-for-service models.

selvita.com
2Drug Development Services
TypeProfessional Services
Description

CMC analytical services, formulation development, GMP manufacturing, stability studies, quality control and QP release for small molecules and biologics under GMP/GLP standards.

selvita.com
3Contract Testing Services
TypeProfessional Services
Description

GxP-compliant analytical testing services including method development, validation, impurity profiling, and bioanalysis for pharmaceutical and agrochemical clients.

selvita.com
4Regulatory Affairs
TypeProfessional Services
Description

Regulatory support for European market approval including dossier preparation, clinical trial applications, and registration services.

prnewswire.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

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

Cost components5 values
Personnel, Technology or R&D, Operations, Infrastructure, Marketing or Sales
Pricing details1 tier
1FTE (Full-Time Equivalent) model - dedicated team allocation
ModelOtherBilling cadenceMulti-year contract
Notes

Flexible engagement model where clients can dedicate full-time equivalent researchers to projects

selvita.com
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

Selvita is an integrated contract research organization (CRO) providing drug discovery and drug development services to pharmaceutical and biotech companies. Service offerings span target validation through preclinical candidate nomination for small molecules, antibodies, and protein degraders, plus CMC analytical, formulation, GMP manufacturing, regulatory affairs, and GLP-compliant agroscience testing. Delivery models include both standalone studies and fully integrated discovery and development programs under FTE or fee-for-service contracts.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Selvita is an integrated drug discovery and development service provider organized around three core service pillars: Drug Discovery Services, Drug Development Services, and specialized Agroscience Services. The Drug Discovery pillar encompasses AI-powered virtual screening (TADAM platform), computer-aided drug design, medicinal chemistry, protein sciences, pharmacology, DMPK, and omics capabilities. The Drug Development pillar provides CMC analytical services, formulation development, GMP manufacturing, quality control, and regulatory affairs support for small molecules and biologics. Specialty areas include nitrosamine/impurities testing, solid-state characterization, and scale-up chemistry. The company operates under GMP and GLP standards across facilities in Poland and Croatia, offering both standalone studies and fully integrated discovery and development programs.

Product and service7 records
1Drug Discovery Services
CategoryCore Service
Description

Integrated drug discovery services from target validation to preclinical candidate nomination, supporting small molecules, antibodies, and protein degraders. Delivered via standalone studies or fully integrated discovery programs under FTE or fee-for-service models. For pharmaceutical and biotech companies.

2Drug Development Services
CategoryCore Service
Description

End-to-end drug development and regulatory support including analytical services for small and large molecules, microbiology, formulation, and clinical trial batch manufacturing under GMP and GLP regulations. For pharmaceutical and biotech companies.

3Antibody Discovery Services
CategoryCore Service
Description

Comprehensive antibody discovery including phage display libraries, antibody engineering, developability assessment, characterization, and bispecific antibody development. For biotech and pharmaceutical companies developing antibody therapeutics.

4Biologics Development Services
CategoryCore Service
Description

Analytical services for biologics including protein characterization, immunogenicity testing, bioassays, biosimilarity assessment, and support for advanced modalities such as ADCs and oligonucleotides. For pharmaceutical and biotech companies.

5Agroscience Services
CategoryCore Service
Description

GLP-compliant analytical services for crop protection agents including method development, physicochemical testing, impurity profiling, residue analysis, and certification. For agrochemical companies requiring product registration support.

6CPSA Target Engagement Technology
CategoryTechnology Platform
Description

Cellular Protein Structural Analysis (CPSA) - proprietary target engagement technology that measures drug-target interactions directly in cellular lysates. Offers simple, cost-effective, and scalable solution for assessing target engagement during drug discovery with comparable pharmacology to existing assays. For pharmaceutical and biotech researchers.

7Clinical Supply GMP Manufacturing
CategoryCore Service
Description

Clinical supply GMP manufacturing of drug substance and drug product for early-stage clinical trials, including formulation development and packaging. For pharmaceutical companies preparing clinical-stage molecules.

Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
1Llamatech Nanobody Solutions
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-06-02
Description

Selvita expanded its antibody discovery portfolio through collaboration with Llamatech Nanobody Solutions, enabling enhanced capabilities in nanobody-based therapeutics development.

selvita.com
Recent move15 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Global CDMO providing development and manufacturing services for small molecules, biologics, and cell/gene therapies. Overlaps with Selvita's Drug Development and biologics CMC services via PozLab, but operates at vastly larger scale and across more modalities.

TypeBroad incumbent
Description

Largest global CRO with integrated clinical and R&D services, including laboratory, data, and technology capabilities. Competes with Selvita in early-phase research services but is far broader, with dominant clinical trial capabilities and technology platforms.

TypeDirect peer
Description

Asia-headquartered CRO providing integrated drug discovery, medicinal chemistry, biology, and DMPK services to global pharma. Directly comparable to Selvita's core discovery service offering and target customer base, with similar FTE-based engagement model.

TypeDirect peer
Description

UK-based integrated drug discovery CRO offering medicinal chemistry, biology, DMPK, and computational chemistry services. Closely comparable to Selvita in scale, geographic base (UK/Europe), and integrated discovery service model.

TypeBroad incumbent
Description

Mid-to-large CRO focused on clinical development for small and mid-sized biopharma. Less directly comparable in early discovery but competes for integrated outsourced R&D budgets at the same biotech customer segment as Selvita.

TypeDirect peer
Description

European-headquartered integrated drug discovery CRO offering medicinal chemistry, biology, DMPK, and integrated discovery partnerships to pharma/biotech. Directly comparable to Selvita in business model, service scope, and target customer base, though materially larger in scale.

TypeBroad incumbent
Description

China-based global CRO/CDMO providing discovery, preclinical, and manufacturing services across small and large molecules. Directly competes with Selvita in integrated discovery and DMPK services and is far larger in scale and geographic reach.

TypeDirect peer
Description

Global testing, laboratory, and CRO services provider with significant central laboratory and bioanalytical testing capabilities. Comparable to Selvita's Drug Development segment (CMC analytical, bioanalysis, GMP/GLP testing) and increasingly overlapping in early discovery services.

TypeDirect peer
Description

China-headquartered CRO/CDMO providing integrated drug discovery, preclinical, CMC, and manufacturing services to global pharma. Closely comparable to Selvita in integrated discovery-plus-development positioning, with overlapping services in medicinal chemistry, DMPK, and biologics.

TypeBroad incumbent
Description

Large global CRO offering discovery, safety assessment, and manufacturing services with strong presence in preclinical research. Comparable to Selvita's discovery and toxicology/safety assessment services but at vastly larger scale and broader geographic reach.

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 customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 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
No

Docs URL, Description

AI capability9 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

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

Subsidiaries3 records

Each record includes

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

Compliance2 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&A2 records

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 →

Selvita

Contract Research Organization (CRO) Servicesselvita.com

Selvita is a Poland-headquartered, publicly listed CRO delivering integrated drug discovery, drug development, and GxP-compliant analytical services to pharmaceutical, biotechnology, and agrochemical clients worldwide.

What Selvita does

Selvita S.A. is a Poland-headquartered, publicly listed contract research organization (CRO) founded in 2007 and traded on the Warsaw Stock Exchange (WSE:SLV). Following a 2019 corporate split that separated proprietary oncology drug discovery into Ryvu Therapeutics, Selvita has operated as a pure-play CRO delivering integrated drug discovery and drug development services to pharmaceutical and biotechnology companies across Europe, North America, and Asia. The company employs more than 950 scientists across research facilities in Kraków, Poznań, and Wrocław (Poland) and Zagreb (Croatia), with commercial subsidiaries in Boston, San Francisco, and Cambridge UK, and serves smaller agrochemical clients through a GLP-compliant analytical testing arm.

The company's core offering is organized into three pillars: Drug Discovery (target validation through preclinical candidate nomination across small molecules, antibodies, and protein degraders), Drug Development (CMC analytical services, formulation, GMP manufacturing, stability studies, QP release, and regulatory affairs under GMP/GLP), and Contract Testing (GxP-compliant analytical services for pharma and agrochemical clients). Underlying the discovery pillar is an integrated technology stack that includes the proprietary TADAM deep-learning virtual screening model (processing 50M+ compounds per hour on NVIDIA H100 GPUs), structure-based drug design with advanced molecular dynamics, CADD/AI for ADMET and selectivity prediction, protein sciences (X-ray, cryo-EM, fragment-based discovery), high-content screening with computer vision, and a multi-omics hub covering genomics, transcriptomics, proteomics, and metabolomics. Recent platform additions include the CPSA cellular target engagement technology (launched November 2025) and a nanobody discovery partnership with Llamatech (June 2026).

Selvita monetizes via professional-services engagements delivered under full-time equivalent (FTE) or fee-for-service contracts of multi-year duration, with global regulatory compliance (FDA, EMA, ICH) and full IP retention by the client as standard terms. The company has scaled through a combination of organic expansion (Hexagon headquarters in Kraków 2023, Wrocław site 2024, US/UK subsidiaries from 2015-2016) and targeted M&A (BioCentrum 2008, Fidelta from Galapagos 2021, PozLab 2024), funded by a 2014 IPO (PLN 27.3M) and a 2020 secondary offering (EUR 20.6M). Most recently, Q1 2026 operating revenues were EUR 19.1M at a 14% EBITDA margin, with Drug Development growing 6% YoY while Drug Discovery declined against a softer European outsourced discovery market.

Selvita firmographics

Firmographics
Name
Selvita
Legal name
Selvita S.A.
Website
https://selvita.com
Company type
Public
Founded year
2007
Operating status
Operating
Headcount range
1,001–5,000 employees
Short description
Selvita is a Poland-headquartered, publicly listed CRO delivering integrated drug discovery, drug development, and GxP-compliant analytical services to pharmaceutical, biotechnology, and agrochemical clients worldwide.
Ownership category
akta.pro rank

Selvita industry classification

Industry
Product category
Contract Research Organization (CRO) Services
NAICS
Scientific Research and Development Services (5417), Testing Laboratories and Services (54138)
SIC
Services-Commercial Physical & Biological Research (8731), Services-Testing Laboratories (8734)
akta.pro industry
PRIMARYHLAGAAAB
Preclinical CROs (Discovery/Pharmacology/DMPK)
SECONDARYHLAGAAAC
Toxicology & Safety Assessment CROs (GLP)
SECONDARYHLAGAAAE
Central Laboratory & Clinical Trial Testing CROs
SECONDARYHLAGAOAE
Quality Assurance, GxP Compliance & Auditing FSP
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Scientific Staffing & Functional Service Providers (FSP)

Keywords

  • Contract research services
  • Drug discovery services
  • Preclinical drug development
  • Medicinal chemistry services
  • Pharmaceutical R&D outsourcing

Where Selvita is headquartered

Location

Headquarters

HQ city
Kraków
HQ country
Poland
HQ region
Europe

Offices7 records

Markets served

Selvita business model

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

Revenue model

  1. Drug Discovery Services: Integrated or standalone solutions spanning medicinal chemistry, biology, DMPK, and protein sciences from target validation to preclinical candidate nomination. Delivered via FTE or fee-for-service models.
  2. Drug Development Services: CMC analytical services, formulation development, GMP manufacturing, stability studies, quality control and QP release for small molecules and biologics under GMP/GLP standards.
  3. Contract Testing Services: GxP-compliant analytical testing services including method development, validation, impurity profiling, and bioanalysis for pharmaceutical and agrochemical clients.
  4. Regulatory Affairs: Regulatory support for European market approval including dossier preparation, clinical trial applications, and registration services.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractFTE (Full-Time Equivalent) model - dedicated team allocation

Go-to-market motion2 records

Distribution channels4 records

Marketing channels6 records

Selvita product offering

Product offering

Core offering

Selvita is an integrated contract research organization (CRO) providing drug discovery and drug development services to pharmaceutical and biotech companies. Service offerings span target validation through preclinical candidate nomination for small molecules, antibodies, and protein degraders, plus CMC analytical, formulation, GMP manufacturing, regulatory affairs, and GLP-compliant agroscience testing. Delivery models include both standalone studies and fully integrated discovery and development programs under FTE or fee-for-service contracts.

Product overview

Selvita is an integrated drug discovery and development service provider organized around three core service pillars: Drug Discovery Services, Drug Development Services, and specialized Agroscience Services. The Drug Discovery pillar encompasses AI-powered virtual screening (TADAM platform), computer-aided drug design, medicinal chemistry, protein sciences, pharmacology, DMPK, and omics capabilities. The Drug Development pillar provides CMC analytical services, formulation development, GMP manufacturing, quality control, and regulatory affairs support for small molecules and biologics. Specialty areas include nitrosamine/impurities testing, solid-state characterization, and scale-up chemistry. The company operates under GMP and GLP standards across facilities in Poland and Croatia, offering both standalone studies and fully integrated discovery and development programs.

Differentiator

Problem solved

Functional benefit

Products and services

  • Drug Discovery Services Integrated drug discovery services from target validation to preclinical candidate nomination, supporting small molecules, antibodies, and protein degraders. Delivered via standalone studies or fully integrated discovery programs under FTE or fee-for-service models. For pharmaceutical and biotech companies.
  • Drug Development Services End-to-end drug development and regulatory support including analytical services for small and large molecules, microbiology, formulation, and clinical trial batch manufacturing under GMP and GLP regulations. For pharmaceutical and biotech companies.
  • Antibody Discovery Services Comprehensive antibody discovery including phage display libraries, antibody engineering, developability assessment, characterization, and bispecific antibody development. For biotech and pharmaceutical companies developing antibody therapeutics.
  • Biologics Development Services Analytical services for biologics including protein characterization, immunogenicity testing, bioassays, biosimilarity assessment, and support for advanced modalities such as ADCs and oligonucleotides. For pharmaceutical and biotech companies.
  • Agroscience Services GLP-compliant analytical services for crop protection agents including method development, physicochemical testing, impurity profiling, residue analysis, and certification. For agrochemical companies requiring product registration support.
  • CPSA Target Engagement Technology Cellular Protein Structural Analysis (CPSA) - proprietary target engagement technology that measures drug-target interactions directly in cellular lysates. Offers simple, cost-effective, and scalable solution for assessing target engagement during drug discovery with comparable pharmacology to existing assays. For pharmaceutical and biotech researchers.
  • Clinical Supply GMP Manufacturing Clinical supply GMP manufacturing of drug substance and drug product for early-stage clinical trials, including formulation development and packaging. For pharmaceutical companies preparing clinical-stage molecules.

Companies that use Selvita

Customer profile

Named customers1 record

Segments3 records

Ideal customer profiles3 records

Selvita technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability9 records

Feature5 records

Selvita partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Llamatech Nanobody SolutionscoreStrategic or Co-development Partner · 2 June 2026Selvita expanded its antibody discovery portfolio through collaboration with Llamatech Nanobody Solutions, enabling enhanced capabilities in nanobody-based therapeutics development.

Scale indicators9 records

Recent moves15 records

Expansion highlights6 records

Selvita competitors and assessment

Company assessment

Broad incumbents

  • Lonza Group: Global CDMO providing development and manufacturing services for small molecules, biologics, and cell/gene therapies. Overlaps with Selvita's Drug Development and biologics CMC services via PozLab, but operates at vastly larger scale and across more modalities.
  • IQVIA: Largest global CRO with integrated clinical and R&D services, including laboratory, data, and technology capabilities. Competes with Selvita in early-phase research services but is far broader, with dominant clinical trial capabilities and technology platforms.
  • Medpace Holdings: Mid-to-large CRO focused on clinical development for small and mid-sized biopharma. Less directly comparable in early discovery but competes for integrated outsourced R&D budgets at the same biotech customer segment as Selvita.
  • WuXi AppTec: China-based global CRO/CDMO providing discovery, preclinical, and manufacturing services across small and large molecules. Directly competes with Selvita in integrated discovery and DMPK services and is far larger in scale and geographic reach.
  • Charles River Laboratories: Large global CRO offering discovery, safety assessment, and manufacturing services with strong presence in preclinical research. Comparable to Selvita's discovery and toxicology/safety assessment services but at vastly larger scale and broader geographic reach.

Direct peers

  • ChemPartner: Asia-headquartered CRO providing integrated drug discovery, medicinal chemistry, biology, and DMPK services to global pharma. Directly comparable to Selvita's core discovery service offering and target customer base, with similar FTE-based engagement model.
  • Sygnature Discovery: UK-based integrated drug discovery CRO offering medicinal chemistry, biology, DMPK, and computational chemistry services. Closely comparable to Selvita in scale, geographic base (UK/Europe), and integrated discovery service model.
  • Evotec SE: European-headquartered integrated drug discovery CRO offering medicinal chemistry, biology, DMPK, and integrated discovery partnerships to pharma/biotech. Directly comparable to Selvita in business model, service scope, and target customer base, though materially larger in scale.
  • Eurofins Scientific: Global testing, laboratory, and CRO services provider with significant central laboratory and bioanalytical testing capabilities. Comparable to Selvita's Drug Development segment (CMC analytical, bioanalysis, GMP/GLP testing) and increasingly overlapping in early discovery services.
  • Pharmaron: China-headquartered CRO/CDMO providing integrated drug discovery, preclinical, CMC, and manufacturing services to global pharma. Closely comparable to Selvita in integrated discovery-plus-development positioning, with overlapping services in medicinal chemistry, DMPK, and biologics.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

Selvita social profiles

Digital presence

Selvita compliance and trust

Trust signal

Compliance2 records

Selvita financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Selvita leadership team

Management profile

Number of profiles

Profiles3 records

Selvita subsidiaries and ownership

Company hierarchy

Subsidiaries3 records

Selvita funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Selvita M&A and investment

M&A and investment

M&A2 records

Investments

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

Frequently asked questions about Selvita

What does Selvita do?

Selvita is an integrated contract research organization (CRO) providing drug discovery and drug development services to pharmaceutical and biotech companies. Service offerings span target validation through preclinical candidate nomination for small molecules, antibodies, and protein degraders, plus CMC analytical, formulation, GMP manufacturing, regulatory affairs, and GLP-compliant agroscience testing. Delivery models include both standalone studies and fully integrated discovery and development programs under FTE or fee-for-service contracts.

Is Selvita a public or private company?

Selvita is a public company. It is classified as public and is currently operating.

When was Selvita founded?

Selvita was founded in 2007. It employs 1,001 to 5,000 people.

Where is Selvita based?

Selvita is headquartered in Kraków, Poland, in the Europe region.

How does Selvita make money?

Four revenue lines are on record. Drug Discovery Services are the primary driver. The others are drug Development Services, contract Testing Services and regulatory Affairs.

Who are Selvita's main competitors?

Broad incumbents on record are Lonza Group, IQVIA, Medpace Holdings, WuXi AppTec and Charles River Laboratories. Direct peers are ChemPartner, Sygnature Discovery, Evotec SE, Eurofins Scientific and Pharmaron.

Does Selvita have an API?

No public API is recorded for Selvita.

What industry is Selvita in?

Selvita's product category is Contract Research Organization (CRO) Services. Its primary akta.pro industry code is HLAGAAAB, Preclinical CROs (Discovery/Pharmacology/DMPK), with a secondary code of HLAGAAAC, Toxicology & Safety Assessment CROs (GLP). Its NAICS code is 5417 and its SIC code is 8731.

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Live signals
PR NewswireSelvita reports Q1 2026 results and launches strategic options reviewSelvita S.A., a European Drug Discovery and Development organization listed on the Warsaw Stock Exchange, reported Q1 2026 operating revenues of EUR 19.1 million with a 14% EBITDA margin, a decline from EUR 21.8 million in the prior year driven by a challenging European outsourced drug discovery services market and project delays. The company announced a broad strategic options review to potentially include a take-private transaction or accelerated M&A and organic growth, with Rothschild & Co engaged as financial adviser. The Drug Development segment showed 6% year-over-year revenue growth to EUR 6.2 million and represents a key growth driver, while the Drug Discovery segment experienced a decline to EUR 11.6 million from EUR 15.6 million.AD HOC NEWSSelvita S.A. stock (PLSEV0000014): Biotech firm eyes growth in drug discovery servicesSelvita S.A. is a Polish contract research organization (CRO) providing integrated drug discovery and development services to pharmaceutical and biotech clients across Europe, North America, and Asia. The company reported revenue growth in 2025 driven by an expanding portfolio of discovery and development contracts, particularly in oncology, inflammation, and central nervous system disorders. Selvita continues to invest in laboratory infrastructure and digital tools to support its platform while positioning itself to benefit from ongoing pharmaceutical R&D outsourcing trends.openPR.comIn-Depth Examination of Segments, Industry Trends, and Key Competitors in the Drug Discovery Outsourcing MarketThe drug discovery outsourcing market is projected to grow to $6.15 billion by 2030, with a compound annual growth rate of 7.7%, driven by AI adoption, personalized medicine, and globalization of pharmaceutical R&D. In July 2024, Poland-based Selvita SA acquired PozLab to enhance its end-to-end pharmaceutical development and small molecule drug manufacturing capabilities for early clinical trials. Additionally, in April 2024, Thermo Fisher Scientific launched the iCAP PRO XP ICP-OES with Semi-Quantification Analysis technology for faster elemental detection in laboratory settings.Data Insights MarketIn-Silico Drug Discovery Trends and Forecasts: Comprehensive InsightsA market research report on the in-silico drug discovery sector estimates the market at $15.13 billion in 2025, projecting a compound annual growth rate (CAGR) of 7.48% through 2033, driven by AI and machine learning integration, increased R&D collaborations, and the need for cost-effective pharmaceutical development. North America is expected to lead the market due to its high concentration of pharmaceutical companies, strong research infrastructure, and high adoption of advanced technologies, while Europe and Asia-Pacific are also poised for significant growth. Key players identified in the report include Charles River, Certara, Evotec, Schrödinger, Dassault Systemes (Biovia), Albany Molecular Research Inc. (AMRI), Selvita, GVK BIO, OpenEye Scientific Software, and Chemical Computing Group (CCG), with moderate M&A activity observed as larger companies acquire specialized in-silico firms to expand capabilities.SelvitaAntibody Characterization MethodsSelvita conducted a comprehensive characterization of the monoclonal antibody Rituximab to evaluate its binding properties and therapeutic mechanisms. The study confirmed that Rituximab binds specifically to human CD20 antigens with high affinity and demonstrates functional efficacy through apoptosis induction and Antibody-Dependent Cellular Cytotoxicity (ADCC).News-MedicalRedefining target engagement with new strategies in drug discoveryA poster originally authored by researchers Paulina Chorobik, Maciej B. Olszewski, John Vincent, and Kirsty Winn was presented at ELRIG Drug Discovery 2025, describing a Chemical Protein Stability Assay (CPSA) for measuring drug-target interactions in cellular lysates during early-stage drug discovery. The CPSA technology, licensed to Selvita from Medicines Discovery Catapult, demonstrated comparable pharmacology and data quality to existing thermal denaturation assays while offering cost-effectiveness and HTS compatibility across 384 and 1536-well formats. Selvita indicated it has successfully applied CPSA across multiple protein targets and continues collaborating with Medicines Discovery Catapult to broaden the technology's applications in drug discovery programs.YahooDrug Discovery Services Company Evaluation Report 2025 | LabCorp, Evotec, and Selvita Lead with Comprehensive Research and Laboratory ServicesMarketsandMarkets 360 Quadrants released a drug discovery services company evaluation report, evaluating over 150 companies and identifying the top 25. LabCorp, Evotec, and Selvita are highlighted as leading providers, with growth driven by rising R&D investments and outsourcing demand.PR NewswireSelvita Reports Rebound in H2 2024 and 11% Increase in Backlog for 2025Selvita S.A. reported strong H2 2024 performance with Q4 commercial revenues of EUR 22.5 million, up 14% year-over-year, and EBITDA of EUR 4.8 million, up 26% y/y with a 21.1% margin. The company's backlog for 2025 stands at EUR 51 million, an 11% year-over-year increase, while big pharma customers now represent 26% of total revenue following a 51% y/y increase in revenues from this segment. Management expressed confidence in continued growth but noted recent slowdown in customer decision-making due to macroeconomic uncertainty.PR NewswireSelvita completes acquisition of PozLab and significantly expands its drug development capabilitiesSelvita S.A., a Polish preclinical contract research organization listed on the Warsaw Stock Exchange, has completed its acquisition of 100% of shares in PozLab, a contract development and manufacturing organization (CDMO) based in Poznan, Poland. PozLab brings GMP-licensed drug product development capabilities including analytical, formulation, and process development services, as well as microbiological testing, and employs over 80 subject matter experts across approximately 1,700 square meters of R&D facilities. The acquisition extends Selvita's value chain beyond preclinical research into small molecule drug manufacturing for early-stage clinical trials, positioning the company as a comprehensive solution provider in the pharmaceutical industry.PR NewswireSelvita launches biologic drug discovery and development servicesSelvita S.A., a Polish preclinical contract research organization listed on the Warsaw Stock Exchange, announced a strategic expansion into biologic drug discovery and development services by adding therapeutic antibody discovery capabilities to its portfolio. The company will open a new research site in Wroclaw, Poland, renting over 400 sq m of state-of-the-art laboratories and initially contracting 16 experienced scientists formerly at Pure Biologics, with plans to double headcount within three years. This expansion complements Selvita's existing small molecule and protein chemistry offerings, positioning the company to offer comprehensive "All Under One Roof" protein services across both small molecules and biological drugs.