Extrovis
Extrovis AG is an Indo-Swiss global CRDMO headquartered in Switzerland that develops and manufactures complex therapeutics, including sterile antibiotics, cytotoxic formulations, peptides, and drug-device combinations, for global pharmaceutical companies across 50+ countries via a five-country manufacturing and R&D network.
- Company typePrivate
- Founded-
- HeadquartersBaar, Switzerland
- Headcount51–100
- GTM typeB2B
- OfferingServices
What Extrovis does
Extrovis AG is an Indo-Swiss global Contract Research, Development and Manufacturing Organization (CRDMO) headquartered in Baar, Switzerland, that develops and manufactures complex therapeutics for the world's pharmaceutical companies. The company is structured around five operating geographies: corporate headquarters in Switzerland, R&D centers in Hyderabad and Pune (India), manufacturing operations at Latina Pharma in Italy, Pharma Pack in Hungary, and the flagship Kavis Pharma facility in Sugar Land, Texas. As of 2026 it employs 750+ professionals, including 250+ R&D scientists across three continents, delivering against a portfolio that spans sterile antibiotics (cephalosporins APIs and dosage forms, monobactams), cytotoxic formulations across OEB 1-5 (oral solids, injectables, topicals, oral liquids), and female hormone products, alongside newer modalities such as drug-device combinations, peptides, and complex parenterals.
The company's core technology platform is its multi-jurisdictional manufacturing infrastructure accredited by US FDA, EU GMP, and PMDA, with dedicated segregated production lines for beta-lactams and engineered containment for high-potent compounds. R&D capabilities span formulation development, novel delivery systems, and advanced process analytical technologies, supporting delivery of 50+ dosage forms and 30+ drug substances from concept through commercialization. An integrated global supply chain serves 200+ SKUs across 50+ countries, with capabilities anchored in Research, Manufacturing, and Commercial functions.
Commercially, Extrovis operates a B2B enterprise contract services model, generating revenue through transaction fees on contract manufacturing and professional services fees on R&D and regulatory engagements. Pricing is quote-based and project-negotiated, tied to complexity, volume, and regulatory requirements, and is not publicly disclosed. The go-to-market motion targets both large global pharma companies and small biotech sponsors through long-term strategic alliances built on 'accountable collaboration models.' Distribution is exclusively direct, with no intermediary channels, supported by digital marketing (corporate website, LinkedIn, Facebook), email inquiry, and industry events. Registered sub-brands SOLARTUS and ADROIQ suggest pending branded product initiatives beyond core contract services.
Extrovis firmographics
Firmographics- Name
- Extrovis
- Legal name
- Extrovis AG
- Website
- https://extrovis.com
- Company type
- Private
- Operating status
- Operating
- Headcount range
- 51–100 employees
- Short description
- Extrovis AG is an Indo-Swiss global CRDMO headquartered in Switzerland that develops and manufactures complex therapeutics, including sterile antibiotics, cytotoxic formulations, peptides, and drug-device combinations, for global pharmaceutical companies across 50+ countries via a five-country manufacturing and R&D network.
- Ownership category
- akta.pro rank
Extrovis industry classification
Industry- Product category
- Pharmaceutical CDMO Services
- NAICS
- Pharmaceutical Preparation Manufacturing (325412), Pharmaceutical and Medicine Manufacturing (3254), Scientific Research and Development Services (5417)
- SIC
- Pharmaceutical Preparations (2834)
- akta.pro primary industry
- Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC) (HLAGAHAM)
- akta.pro secondary industries
- Regulatory Strategy & Global Submissions (IND/CTA/NDA/BLA/MAA) (HLAGAKAA), Clinical CROs (Phase I–IV) (HLAGAAAA)
Keywords
Where Extrovis is headquartered
LocationHeadquarters
- HQ city
- Baar
- HQ country
- Switzerland
- HQ region
- Europe
Offices8 records
Markets served
Extrovis business model
Business model- GTM type
- B2B
- Offering type
- Services
- Cost components
- Personnel, Operations, Infrastructure, Technology or R&D, Supply Chain, Marketing or Sales
Revenue model
- Contract Manufacturing Services: CDMO revenue from manufacturing drug substances and drug products for pharmaceutical partners. Services span from clinical development through commercial scale with regulated market supply. Revenue generated through project-based contracts with pharmaceutical companies for development and manufacturing services.
- Contract Research Services: R&D services including formulation development, process design, and primary packaging for pharmaceutical companies. Global R&D organization delivers dosage forms and drug substances from concept through scale-up and regulatory approval.
- Regulatory Services: Regulatory affairs support enabling faster approvals through compliant submissions. Expertise in country-specific requirements and filings for global market entry.
Go-to-market motion2 records
Distribution channels2 records
Marketing channels5 records
Extrovis product offering
Product offeringCore offering
Extrovis is a global Contract Research, Development, and Manufacturing Organization (CRDMO) providing integrated pharmaceutical services from molecule to market. The company specializes in sterile antibiotics (APIs and dosage forms), cytotoxic oncology formulations (oral solids, injectables, topicals, oral liquids), and female hormone products. Services span formulation R&D, drug substance and drug product manufacturing, regulatory submissions, and global supply chain distribution across USFDA-, EU-GMP-, and PMDA-accredited facilities.
Product overview
Extrovis is an Indo-Swiss global CRDMO (Contract Research, Development & Manufacturing Organization) that operates as a unified platform offering integrated pharmaceutical development and manufacturing services. The company's portfolio comprises two core service lines: Drug Substances (Sterile Cephalosporins, High Potent Monobactams, Advanced Intermediates, and Controlled Substances) and Drug Products (Oncology Solids, Oncology Injectables, Oncology Topicals, Oncology Oral Liquids, Cephalosporin Injectable Vials, Cephalosporin Dual Chamber Bags, Female Hormone Topicals, Oral Liquids, and General Topicals). These capabilities are supported by R&D Services for formulation development and novel delivery systems, Manufacturing Services leveraging US FDA, EU GMP, and PMDA-accredited facilities, and Global Supply Chain Services covering 50+ markets with 200+ SKUs. The company specializes in high-impact therapeutic areas including oncology, sterile antibiotics and anti-infectives, and high-containment complex manufacturing.
Differentiator
Problem solved
Functional benefit
Brands
- SOLARTUS: Registered trademark of Extrovis AG and/or its affiliates.
- ADROIQ
Products and services
- Drug Substance Manufacturing Services
Quantifiable outcome
- Delivered 50+ dosage forms and 30+ drug substances from concept through commercialization
- +2 more outcomes
Companies that use Extrovis
Customer profileNamed customers1 record
Segments2 records
Ideal customer profiles2 records
Extrovis technology and API
TechnologyTechnology focussed No
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature12 records
Extrovis partnerships and signals
Strategic signalScale indicators8 records
Recent moves5 records
Expansion highlights6 records
Extrovis competitors and assessment
Company assessmentDirect peers
- Recipharm: European-headquartered CDMO with sterile fill-finish, API and oral solid dose capabilities — comparable in contract manufacturing scope, with a stronger European footprint and weaker India base.
- Syngene International: Bengaluru-based CRDMO providing API development, formulation and contract manufacturing to global pharma — comparable in Indo-global CRDMO model, though with a heavier discovery/CRO tilt than Extrovis.
- Piramal Pharma Solutions: India-headquartered global CDMO offering integrated drug substance and drug product development and manufacturing across sterile injectables, high-potency APIs and oral solids — directly comparable to Extrovis' CRDMO service mix and Indo-Swiss positioning.
- Sai Life Sciences: India-based CRDMO offering API, intermediate and formulation services to global innovator and generic pharma — directly comparable small-molecule development and manufacturing capability to Extrovis.
- Hikal: Indian CRDMO with API, intermediates and custom manufacturing across therapeutics including cephalosporins — directly comparable in geographic mix and small-molecule/API focus.
- Jubilant Pharmova: India-listed pharma company with a CDMO segment covering sterile injectables, APIs and radiopharmaceuticals — comparable in Indo-global CRDMO model with regulated-market supply.
- WuXi STA (WuXi AppTec): China-based global CRDMO with end-to-end API and drug product services across small molecules, peptides and complex injectables — directly comparable CRDMO service model, though currently exposed to US BIOSECURE-related headwinds.
Broad incumbents
- Lonza: Swiss-headquartered global CDMO leader across small molecules, biologics and cell/gene therapy — overlaps with Extrovis on small-molecule API and drug product, but at materially larger scale and broader modality coverage.
- Aurobindo Pharma: Large Indian generics manufacturer with growing CMO/CDMO services across APIs, injectables and cephalosporins — comparable in therapeutic focus but operates as a broad incumbent with much larger revenue base than Extrovis.
- Catalent: Global CDMO leader in softgel, oral and biologics fill-finish — overlapping capabilities in complex drug product development but with a much broader portfolio and recent Novo Holdings take-private.
Market position
Strengths5 records
Weaknesses4 records
Competitive moat6 records
Key risks6 records
Key highlights6 records
Customer concentration
Extrovis social profiles
Digital presenceExtrovis financial estimates
Financial estimateRevenue estimate
Valuation estimate
Extrovis leadership team
Management profileNumber of profiles
Profiles13 records
Extrovis subsidiaries and ownership
Company hierarchySubsidiaries4 records
Extrovis funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Extrovis 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 Extrovis
What does Extrovis do?
Extrovis is a global Contract Research, Development, and Manufacturing Organization (CRDMO) providing integrated pharmaceutical services from molecule to market. The company specializes in sterile antibiotics (APIs and dosage forms), cytotoxic oncology formulations (oral solids, injectables, topicals, oral liquids), and female hormone products. Services span formulation R&D, drug substance and drug product manufacturing, regulatory submissions, and global supply chain distribution across USFDA-, EU-GMP-, and PMDA-accredited facilities.
Is Extrovis a public or private company?
Extrovis is a private company. It is classified as unknown and is currently operating.
When was Extrovis founded?
Extrovis was founded in -1. It employs 51 to 100 people.
Where is Extrovis based?
Extrovis is headquartered in Baar, Switzerland, in the Europe region.
How does Extrovis make money?
Three revenue lines are on record. Contract Manufacturing Services are the primary driver. The others are contract Research Services and regulatory Services.
Who are Extrovis's main competitors?
Direct peers on record are Recipharm, Syngene International, Piramal Pharma Solutions, Sai Life Sciences, Hikal, Jubilant Pharmova and WuXi STA (WuXi AppTec). Broad incumbents are Lonza, Aurobindo Pharma and Catalent.
Does Extrovis have an API?
No public API is recorded for Extrovis.
What industry is Extrovis in?
Extrovis's product category is Pharmaceutical CDMO Services. Its primary akta.pro industry code is HLAGAHAM, Small-Molecule CMC Documentation & Regulatory Support (DMF/CMC), with a secondary code of HLAGAKAA, Regulatory Strategy & Global Submissions (IND/CTA/NDA/BLA/MAA). Its NAICS code is 325412 and its SIC code is 2834.