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Solutions
- Clinical Laboratories
  We offer clinical laboratories a wide range of internationally recognised products and services to help them maintain and improve analytical performance.
- Medical Devices
  We provide QARA and clinical research services for the entire lifecycle of a medical device.
- Pharmaceuticals & Biotech
  Our experienced team provides extensive and high-quality services for pharma and biotech companies.
Services
- External Quality Assessment
  Our external quality assessment service program includes more than 250 quality assessment schemes.
- Pharmaceutical CRO services
  We are a full-service CRO working with phases I-IV.
- Medical devices CRO services
  We help medical device companies in meeting the new, comprehensive requirements and compliance expectations during the entire lifecycle of your products
- Regulatory affairs
  Our services cover the entire lifecycle of medical and in vitro diagnostic devices.
- Quality assurance
  Our experienced quality assurance professionals offer flexible services.
Learning
- Clinical investigations
  See trainings related to clinical investigations.
- Regulatory essentials
  This training series provides an efficient introduction to the regulatory essentials to turn regulatory compliance into a business advantage and to avoid the typical pitfalls of the health tech sector.
- Medical devices
  Trainings related to medical devices and regulation.
- ICH GCP
  Good Clinical Practice training
Insights
- Expert perspectives
  Look into current topics in health sector and regulation with our experts.
- News
  The latest news from Aurevia. Keep track of what's happening!
- Events
  Meet us at events.
  - Labquality Days
- Glossary
  Acronyms and terms in clinical research and regulation explained.
- Scientific posters
  See our scientific posters presented at various congresses
- References
  Learn more about the companies we serve and the work we do.
About us
- Our story
  Aurevia formed in January 2025 when Artimed, Clinical Consulting, Kasve, Labquality, and P.R.I.S.M.A. merged as Aurevia.
- Contact us
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- Locations
  Our offices in different countries.
- Careers
  Interested in working with us? Check out our vacancies and apply!

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AUREVIA ACADEMY

Training and events

We offer an even wider range of training services on quality management, patient safety and medical device regulation. Whether you're a quality expert, laboratory professional, development manager or radiology professional, we have the training that's right for you. Secure and maintain your skills!

Early bird discount

If you register at least one month before the course starts, you will receive a 10% discount on the course price with the code EARLY.

Aurevia Academy Training Calendar

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ISO 9001 täydentäminen ISO 14001 standardilla

Time: 27.2.2025 klo 9.00-16.00
Place: Online
Price: 690€ + ALV 25,5%

Introduction to the ISO 13485 Standard

Time: 11/03/2025 from 9 AM to 16 (EET)
Place: Online
Price: 690€ + VAT 25.5%

ISO 9001 -standardin mukainen sisäinen auditointi

Time: 12.3. ja 23.4.2025 klo 9.00-16.00
Place: Online
Price: 890€ + ALV 25,5%

ISO 13485 Standard Internal Auditing

Time: 18/03 and 29/04/2025 from 9 AM to 4 PM (EET)
Place: Online
Price: 690€ + VAT 25.5%

Introduction to ISO 14971:2019

Time: 09/04/2025 from 9 AM to 4 PM (EET)
Place: Online
Price: 690€ + VAT 25.5%

ISO 14001 -standardi tutuksi

Time: 24.4.2025 klo 9.00-16.00
Place: Online
Price: 690€ + ALV 25,5%

Säteilynkäytön sisäinen kliininen auditointi -koulutus

Time: 4.9.2025 klo 8.30-15.00
Place: Online
Price: 690€ + ALV 25,5%

SHQS:n mukainen sisäisten auditoijien koulutus

Time: 9.9. ja 30.10.2025 klo 8.30-15.00
Place: Online
Price: 890€ + ALV 25,5%

ISO 9001 tueksi laaduhallintajärjestelmän hallintaan

Time: 17.9.2025 klo 9.00-16.00
Place: online
Price: 690€ + ALV 25,5%

ISO 9001 ja 14001 sisäinen auditointi

Time: 6.11. ja 4.12.2025 klo 9.00-16.00
Place: Online
Price: 890€ + ALV 25,5%

SHQS-standardiin perustuva laadunhallintakoulutus

Time: 25.11.2025 klo 8.30-15.00
Place: Online
Price: 690€ + ALV 25,5%

Medical Devices

Framework of modern medical software development lifecycle

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Medical Devices

GDPR for Medical Devices

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ISO 13485 -standardi tutuksi

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ISO 13485 -standardin mukainen sisäinen auditointi

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ISO 14001 -standardin mukainen sisäinen auditointi

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ISO 14971:2019 Riskienhallinta

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ISO 22870 standardi tutuksi

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ISO 9001 –standardin sisäisen auditoinnin syventävä koulutus

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Medical Devices

Product safety: Electrical, mechanical, radiation, usability, software

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Medical Devices

Product safety: Electromagnetic Compatibility of electrically operated products

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Medical Devices

Perusteet lääkinnällisten ohjelmistojen kehittämiselle

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Medical Devices

Regulatory Essentials in Health Tech - Full Training Series

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Regulatory Essentials

Regulatory Essentials in Health Tech: Compliance as a Business Advantage

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Regulatory Essentials

Regulatory Essentials in Health Tech: Early Development and Management

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Regulatory Essentials

Regulatory Essentials in Health Tech: The Core of the Regulatory Requirements

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Regulatory Essentials

Regulatory Essentials in Health Tech: Design Control and the Regulatory Environment

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Regulatory Essentials

Regulatory Essentials in Health Tech: Regulatory Essentials of In Vitro Diagnostics

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Regulatory Essentials

Regulatory Essentials in Health Tech: Medical Device Software

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Regulatory Essentials

Regulatory Essentials in Health Tech: Risk Management in Practice

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Regulatory Essentials

Regulatory Essentials in Health Tech: FDA

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Regulatory Essentials

Regulatory Essentials in Health Tech: Usability and Labelling

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Regulatory Essentials

Regulatory Essentials in Health Tech: Biological and Electrical Safety

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Regulatory Essentials

Regulatory Essentials in Health Tech: Clinical Evaluation in Practice

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Regulatory Essentials

Regulatory Essentials in Health Tech: Clinical Investigations in Practice

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Regulatory Essentials

Regulatory Essentials in Health Tech: Post-Market Surveillance and Clinical Follow-up

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Regulatory Essentials

Regulatory Essentials in Health Tech: Person Responsible for Regulatory Compliance

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SFS-EN 15224 -standardi tutuksi

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SFS-EN 15224 -standardin mukainen sisäinen auditointi

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SHQS:n mukainen sisäisten auditoijien täydennyskoulutus

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Medical Devices

Online training on the basics of the IVDR (EU) 2017/746 requirements

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ISO 15189 -standardin mukainen sisäinen auditointi

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ISO 15189:2022 -standardi tutuksi

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ISO/TS 20658 standardi tutuksi

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EKG ja Holter -tutkimukset

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Ulostenäytteenotto

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Histologisten näytteiden ottaminen ja käsittely

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Laskimonäytteenotto

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Lasten näytteenotto

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Mikrobiologiset näytteet

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Spirometria ja bronkodilataatio sekä diffuusiokapasiteetin mittaus

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Virtsanäytteenotto

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Laiteverifiointi ja -validointi– Mitä tulee ottaa huomioon?

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Näkökulmia laiteverifiointeihin – asiantuntijan työkalupakki

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Kvantitatiivisen laitteen verifiointi

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Laiteverifiointien tilastomatematiikka

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Mikrobiologisen laitteen verifiointi

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Mittausepävarmuuden huomioiminen laiteverifioinnissa

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Vieritestauksen sisäinen ja ulkoinen laadunarviointi

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Medical Devices

Clinical evaluation of medical devices according to MDR & MEDDEV 2.7/1 Rev. 4

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Medical Devices

Clinical Research under MDR and ISO 14155:2020

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Medical Devices

PMCF in accordance with MDR and MDCG

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Medical Devices

Publication of clinical study data

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Verenkuvatulosten tulkinta – mitä analysoijan tulee tietää?

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Vieritutkimuspassi: COVID-19

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Vieritutkimuspassi: CRP

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Vieritutkimuspassi: Glukoosi

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Vieritutkimuspassi: INR

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Vieritutkimuspassi: Spiro

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Vieritutkimuspassi: EKG

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Vieritutkimuspassi: HbA1c

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Vieritutkimuspassi: Strep A

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Vieritutkimuspassi: Virtsan liuskakokeet

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EKG-löydösten tunnistaminen

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Gynekologinen näytteenotto

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Clinical Investigations

ICH GCP E6 (R2)

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Medical Devices

Klinische Bewertung von Medizinprodukten (gemäß MDR & MEDDEV 2.7/1 Rev. 4)

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Clinical Investigations

Curricular training for investigators and members of clinical investigation teams/groups

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Clinical Investigations

Curriculare Fortbildungen für Prüfer und Mitglieder eines Prüfungsteams/einer Prüfergruppe

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Medical Devices

Klinische Forschung unter der MDR und ISO 14155

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Medical Devices

PMCF gemäß MDR und MDCG

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Medical Devices

Publikation von Studiendaten

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Poikkeamat muutosvoimaksi

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Lääkinnälliset laitteet

Lääkinnällisten laitteiden kliininen arviointi ja kliiniset laitetutkimukset

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Medical Devices

Health Tech Regulations, Quality Management and Commercialization

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Tehokas muutoksen hallinta

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Vaikuttavan laatukulttuurin rakentaminen

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Lääkinnälliset laitteet

PRRC Connection

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Clinical Investigations

Clinical Investigations 101

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Contact us for more information

Miia Kämppi

Head of Training

miia.kamppi@aurevia.com

+358 40 648 2009

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