Видео ютуба по тегу Technology For Ivdr Compliance

CAPTIS™ - Technology for EU MDR & IVDR Compliance
CAPTIS™ - Technology for EU MDR & IVDR Compliance
CAPTIS™ - Technology for EU MDR & IVDR Compliance
CAPTIS™ - Technology for EU MDR & IVDR Compliance
BEHEALTH 2025 - Panel 1: Medical Devices Regulations (MDR and IVDR): Impacts on Healthcare Systems
BEHEALTH 2025 - Panel 1: Medical Devices Regulations (MDR and IVDR): Impacts on Healthcare Systems
EUDAMED Webinar | MDR & IVDR Compliance Explained
EUDAMED Webinar | MDR & IVDR Compliance Explained
In Vitro Diagnostic Regulation - IVDR
In Vitro Diagnostic Regulation - IVDR
MDR Technical Documentation Requirements | MDR and IVDR Compliance Webinar
MDR Technical Documentation Requirements | MDR and IVDR Compliance Webinar
ESHG IVDR Webinar: Section 3 - IVDR - Obtain regulatory compliance for IH-IVD’s
ESHG IVDR Webinar: Section 3 - IVDR - Obtain regulatory compliance for IH-IVD’s
IVDR compliance: tips and best practice
IVDR compliance: tips and best practice
MDR and IVDR update: Overview and status of EU and national implementation
MDR and IVDR update: Overview and status of EU and national implementation
IVDR Performance Evaluation
IVDR Performance Evaluation
A Roadmap for MDR and IVDR Compliance With QMS
A Roadmap for MDR and IVDR Compliance With QMS
BSI Compliance Navigator | MDR and IVDR – Key changes
BSI Compliance Navigator | MDR and IVDR – Key changes
Understanding the IN VITRO DIAGNOSTIC REGULATION (IVDR) Everything You Need to Know
Understanding the IN VITRO DIAGNOSTIC REGULATION (IVDR) Everything You Need to Know
Implementing and Maintaining PMS and Performance Evaluation under the IVDR – Webinar
Implementing and Maintaining PMS and Performance Evaluation under the IVDR – Webinar
Easy Reference Management with CAPTIS™ - Software for EU MDR and IVDR Compliance
Easy Reference Management with CAPTIS™ - Software for EU MDR and IVDR Compliance
Which devices can be sold as Legacy Devices under IVDR after May 26, 2022?
Which devices can be sold as Legacy Devices under IVDR after May 26, 2022?
How to comply to the GSPR ? (EU MDR and IVDR - Monir El Azzouzi)
How to comply to the GSPR ? (EU MDR and IVDR - Monir El Azzouzi)
Automated Abbreviation Management with CAPTIS™ - Software for EU MDR and IVDR Compliance
Automated Abbreviation Management with CAPTIS™ - Software for EU MDR and IVDR Compliance
IVDR Performance Evaluation IVDs, RUO & In House
IVDR Performance Evaluation IVDs, RUO & In House
Webinar - Ensuring Compliance for your IVD’s Performance Evaluation
Webinar - Ensuring Compliance for your IVD’s Performance Evaluation
IVDR tutorial for diagnostic labs 7: Guidance, concerns, recommendations
IVDR tutorial for diagnostic labs 7: Guidance, concerns, recommendations
How to create your Medical Device Technical File [EU MDR & IVDR]
How to create your Medical Device Technical File [EU MDR & IVDR]
Your Partner for MDR and IVDR Compliance
Your Partner for MDR and IVDR Compliance
IVDR Guidance
IVDR Guidance
EU IVDR: Navigating New Deadlines and Stricter Rules
EU IVDR: Navigating New Deadlines and Stricter Rules