Kasve
Kasve is a Finland-based healthcare consulting firm offering business development, regulatory, quality, and software management services, including the QAiRA tool, to medtech and life sciences clients.
- Company typePrivate
- Founded2012
- HeadquartersKuopio, Finland
- Headcount11–50
- GTM typeB2B
- OfferingServices
What Kasve does
Kasve is a private, for-profit healthcare services firm headquartered in Kuopio, Finland, founded in 2012. The company offers an integrated portfolio of healthcare business development, regulatory affairs, quality management, and software management services, targeting medical device, pharmaceutical, and digital health clients operating in regulated European and adjacent markets. Its service mix combines traditional consulting delivery with QAiRA, a proprietary software tool, suggesting a productized approach to regulatory and quality workflows rather than pure labor-based consulting.
The firm's business model is anchored in professional services revenue with a software component layered on top. Kasve serves a fragmented customer base across healthcare verticals, leveraging regulatory expertise to support clients through complex compliance and market access requirements. With a headcount of 11-50 employees, Kasve operates as a boutique specialist, which positions it to deliver high-touch engagements but constrains scalability relative to larger CRO/QARA consultancies. The company maintains a corporate website (kasve.com) and is privately held with no disclosed funding rounds or institutional investors in the source data.
Direct evidence on Kasve's revenue, customer roster, and pipeline is limited in the supplied material; readers should note that the input also contains detailed data on a separate Sweden-based CRO/QARA firm (Aurevia) which does not appear to pertain to Kasve and has been excluded from this analysis to avoid factual contamination.
Kasve firmographics
Firmographics- Name
- Kasve
- Legal name
- Aurevia
- Website
- https://kasve.com
- Company type
- Private
- Founded year
- 2012
- Operating status
- Operating
- Headcount range
- 11–50 employees
- Short description
- Kasve is a Finland-based healthcare consulting firm offering business development, regulatory, quality, and software management services, including the QAiRA tool, to medtech and life sciences clients.
- Ownership category
- akta.pro rank
Kasve industry classification
Industry- Product category
- Healthcare Regulatory and Quality Consulting
- NAICS
- Professional, Scientific, and Technical Services (54), Computer Systems Design Services (541512)
- SIC
- Services-Computer Processing & Data Preparation (7374)
- akta.pro primary industry
- Quality Engineering & Test Automation (QE/QA) (BPAEAFAJ)
Keywords
Where Kasve is headquartered
LocationHeadquarters
- HQ city
- Kuopio
- HQ country
- Finland
- HQ region
- Europe
Offices1 record
Markets served
Kasve business model
Business model- GTM type
- B2B
- Offering type
- Services
- Cost components
- Personnel, Operations, Technology or R&D, Marketing or Sales, Infrastructure
Revenue model
- CRO Clinical Research Services: Full-service CRO services covering all phases of clinical development for pharma and biotech companies. Services include clinical operations, project management, pharmacovigilance, medical writing, data management, biostatistics, and investigator-initiated trials.
- Quality Assurance and Regulatory Affairs Consulting: Regulatory strategy, market registrations, technical documentation, clinical evaluation, risk management, and QMS services for medical devices and IVDs.
- Training Services (Aurevia Academy): Professional training services within quality assurance, regulatory affairs, and clinical research including seminars, online courses, and tailored training programs.
Go-to-market motion1 record
Distribution channels1 record
Marketing channels6 records
Kasve product offering
Product offeringCore offering
Kasve provides healthcare business development, regulatory affairs, quality management, and software management services to healthcare, pharmaceutical, and medical technology clients. The firm supports clients with regulatory strategy, market access, and quality system needs, and bundles its proprietary QAiRA software tool to operationalize regulatory and quality workflows for healthcare organizations.
Product overview
Aurevia is a full-service consulting company offering a unified portfolio of quality assurance, regulatory affairs, and clinical research services for the pharma, biotech, medtech, and healthcare sectors. The core offerings span four areas of expertise (Medical devices, IVD medical devices, Medical device software, and Pharma & biotech), supported by two main service lines: Pharmaceutical CRO services (covering clinical operations, project management, pharmacovigilance, medical writing, data management, biostatistics, and equipment rental) and Medical device & IVD QARA services (covering regulatory strategy, market registrations, technical documentation, clinical evaluation, risk management, and post-market surveillance). Additional offerings include Aurevia Academy (professional training courses and seminars) and Lean Entries (e-tools for regulatory compliance).
Differentiator
Problem solved
Functional benefit
Brands
- Aurevia Academy: Professional training services within quality assurance, regulatory affairs, and clinical research including seminars, online courses, and tailored training programs.
Products and services
- Healthcare Business Development Services Advisory and execution support to help healthcare, pharmaceutical, biotech, and medtech organizations grow commercially, enter new markets, and develop their healthcare business operations.
- Regulatory Affairs Consulting Regulatory strategy and execution support for healthcare, pharma, biotech, and medtech clients, including navigating complex regulatory requirements and supporting market access.
- Quality Management Services Quality management consulting and execution support for healthcare organizations, including quality system design, implementation, and operational support.
- QAiRA QAiRA is Kasve's proprietary software tool supporting regulatory and quality management workflows for healthcare, pharma, biotech, and medtech clients.
- Healthcare Software Management Services Services to help healthcare organizations manage and operationalize regulatory, quality, and related software tools (including Kasve's QAiRA) within their environments.
Companies that use Kasve
Customer profileNamed customers22 records
Segments5 records
Ideal customer profiles1 record
Kasve technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Kasve partnerships and signals
Strategic signalScale indicators5 records
Recent moves2 records
Expansion highlights2 records
Kasve competitors and assessment
Company assessmentBroad incumbents
- TÜV SÜD: TÜV SÜD is a global testing, inspection, certification, and regulatory body with deep medical device coverage, comparable to Aurevia's IVD/medtech regulatory and quality services.
- ICON plc: ICON is a top-3 global CRO providing clinical operations, biometrics, and consulting to pharma/biotech, comparable to Aurevia's pharma CRO service line but operating at much larger scale.
- IQVIA: IQVIA is a global full-service CRO and life sciences services incumbent; it overlaps Aurevia's pharma/biotech CRO and real-world evidence work but at vastly greater scale across all geographies.
- Medpace: Medpace is a midsized global CRO with full-service clinical development capabilities, directly comparable to Aurevia's pharma CRO offerings across clinical operations, data management, and biostatistics.
- Charles River Laboratories: Charles River provides CRO services plus discovery and safety assessment, overlapping Aurevia's clinical and pharmacovigilance offerings for pharma/biotech sponsors.
- BSI Group: BSI is a global standards, certification, and regulatory services firm with a medical devices notified body, directly comparable to Aurevia's QARA and market-access service lines.
- DEKRA: DEKRA is a global testing and certification organization with a medical/notified body practice, comparable to Aurevia's QARA consulting and EU market access services.
Direct peers
- NAMSA: NAMSA is the leading global medical device-focused CRO and QARA consulting firm, directly comparable to Aurevia's medtech/IVD/SaMD regulatory and clinical research service lines.
- ProPharma Group: ProPharma Group provides pharma and medical device regulatory, compliance, and quality consulting plus clinical services, the closest direct mid-market peer to Aurevia's QARA + CRO combination.
Emerging players
- Premier Research: Premier Research is a midsized CRO focused on specialty pharma and medical device trials, comparable to Aurevia's mid-market CRO positioning in Europe.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat3 records
Key risks7 records
Key highlights6 records
Customer concentration
Kasve social profiles
Digital presenceKasve financial estimates
Financial estimateRevenue estimate
Valuation estimate
Kasve leadership team
Management profileNumber of profiles
Profiles1 record
Kasve funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Kasve 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 Kasve
What does Kasve do?
Kasve provides healthcare business development, regulatory affairs, quality management, and software management services to healthcare, pharmaceutical, and medical technology clients. The firm supports clients with regulatory strategy, market access, and quality system needs, and bundles its proprietary QAiRA software tool to operationalize regulatory and quality workflows for healthcare organizations.
Is Kasve a public or private company?
Kasve is a private company. It is classified as founder individual operated bootstrapped and is currently operating.
When was Kasve founded?
Kasve was founded in 2012. It employs 11 to 50 people.
Where is Kasve based?
Kasve is headquartered in Kuopio, Finland, in the Europe region.
How does Kasve make money?
Three revenue lines are on record. CRO Clinical Research Services are the primary driver. The others are quality Assurance and Regulatory Affairs Consulting and training Services (Aurevia Academy).
Who are Kasve's main competitors?
Broad incumbents on record are TÜV SÜD, ICON plc, IQVIA, Medpace, Charles River Laboratories, BSI Group and DEKRA. Direct peers are NAMSA and ProPharma Group. Premier Research is listed as an emerging player.
Does Kasve have an API?
No public API is recorded for Kasve.
What industry is Kasve in?
Kasve's product category is Healthcare Regulatory and Quality Consulting. Its primary akta.pro industry code is BPAEAFAJ, Quality Engineering & Test Automation (QE/QA). Its NAICS code is 54 and its SIC code is 7374.