Standardi
SHQS-standardin mukainen sisäisen auditoijan koulutus
Time: 9.9. ja 30.10.2025 klo 8.30-15.00
Place: Online
Price: 890€ + ALV 25,5%
Place: Online
Price: 890€ + ALV 25,5%
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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Standardi
ISO 9001 tueksi laadunhallintaan
Time: 17.9.2025 klo 9.00-16.00
Place: online
Price: 690€ + ALV 25,5%
Place: online
Price: 690€ + ALV 25,5%
Standardi
SHQS-standardiin perustuva laadunhallinta sosiaalipalveluissa
Time: 19.9.2025 klo 8.30-15.00
Place: Online
Price: 690€ + alv 25,5%
Place: Online
Price: 690€ + alv 25,5%
Standardi
ISO-standardien mukainen sisäinen auditoija -koulutus
Time: 30.10. ja 4.12.2025 klo 9.00-16.00
Place: Online
Price: 890€ + ALV 25,5%
Place: Online
Price: 890€ + ALV 25,5%
Standardi
SHQS 2.0 -standardiin perustuva laadunhallinta
Time: 25.11.2025 klo 8.30-15.00
Place: Online
Price: 690€ + ALV 25,5%
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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Lääkinnälliset laitteet
ISO 13485 -standardi tutuksi
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Lääkinnälliset laitteet
ISO 13485 -standardin mukainen sisäinen auditointi
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Standardi
ISO 14001 -standardi tutuksi
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Standardi
ISO 14001 -standardin mukainen sisäinen auditointi
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Standardi
ISO 14971:2019 Riskienhallinta
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Standardi
ISO 22870 standardi tutuksi
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Standardi
ISO 9001 –standardin sisäisen auditoinnin syventävä koulutus
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Standardi
ISO 9001 -standardin mukainen sisäinen auditointi
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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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Lääkinnälliset laitteet
Perusteet lääkinnällisten ohjelmistojen kehittämiselle
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Regulatory Essentials
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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Standardi
SFS-EN 15224 -standardi tutuksi
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Standardi
SFS-EN 15224 -standardin mukainen sisäinen auditointi
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Standardi
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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Standardi
Säteilynkäytön sisäinen kliininen auditoijan koulutus
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Lääkinnälliset laitteet
ISO 15189 -standardin mukainen sisäinen auditointi
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Lääkinnälliset laitteet
ISO 15189:2022 -standardi tutuksi
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Standardi
ISO/TS 20658 standardi tutuksi
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Laboratorio
EKG ja Holter -tutkimukset
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Laboratorio
Ulostenäytteenotto
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Laboratorio
Histologisten näytteiden ottaminen ja käsittely
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Laboratorio
Laskimonäytteenotto
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Laboratorio
Lasten näytteenotto
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Laboratorio
Mikrobiologiset näytteet
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Laboratorio
Spirometria ja bronkodilataatio sekä diffuusiokapasiteetin mittaus
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Laboratorio
Virtsanäytteenotto
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Laboratorio
Laiteverifiointi ja -validointi– Mitä tulee ottaa huomioon?
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Laboratorio
Näkökulmia laiteverifiointeihin – asiantuntijan työkalupakki
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Laboratorio
Kvantitatiivisen laitteen verifiointi
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Laboratorio
Laiteverifiointien tilastomatematiikka
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Laboratorio
Mikrobiologisen laitteen verifiointi
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Laboratorio
Mittausepävarmuuden huomioiminen laiteverifioinnissa
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Vieritestaus
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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Clinical Investigations
Publication of clinical study data
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Laboratorio
Verenkuvatulosten tulkinta – mitä analysoijan tulee tietää?
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Vieritestaus
Vieritutkimuspassi: COVID-19
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Vieritestaus
Vieritutkimuspassi: CRP
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Vieritestaus
Vieritutkimuspassi: Glukoosi
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Vieritestaus
Vieritutkimuspassi: INR
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Vieritestaus
Vieritutkimuspassi: Spirometria
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Vieritestaus
Vieritutkimuspassi: EKG
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Vieritestaus
Vieritutkimuspassi: HbA1c
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Vieritestaus
Vieritutkimuspassi: Strep A
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Vieritestaus
Vieritutkimuspassi: Virtsan liuskakokeet
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Laboratorio
EKG-löydösten tunnistaminen
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Laboratorio
Gynekologinen näytteenotto
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Clinical Investigations
ICH GCP E6 (R3)
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Clinical Investigations
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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Standardi
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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Standardi
ISO 9001 täydentäminen ISO 14001 standardilla
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Medical Devices
Introduction to the ISO 13485 Standard
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Medical Devices
ISO 13485 Standard Internal Auditing
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Medical Devices
Introduction to ISO 14971:2019
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Kyberturvallisuus 1: Johdanto kyberturvallisuuteen
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Kyberturvallisuus 2: ISO 27001 –standardi kansantajuisesti
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Kyberturvallisuus 3: ISO 27001 –standardin syventävä koulutus
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Kyberturvallisuus: Kaikki kolme moduulia
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Vieritestaus
Vieritutkimuspassi: Laskimonäytteenotto
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