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IVDR
1:43:11
ESHG IVDR Webinar: Section 1 - Introduction to IVDR
1:03:08
Understanding the IN VITRO DIAGNOSTIC REGULATION (IVDR) Everything You Need to Know
0:02:21
Neue IVDR-Verordnung
2:33:49
IVDR im Fokus – Vorbereitung und kritische Fragen
0:13:18
Everything you need to know about the IVDR
0:35:15
In Vitro Diagnostic Regulation - IVDR
0:00:50
In Vitro Diagnostic Medical Devices Regulation (IVDR) – E-Learning
0:16:24
Clinical Performance under IVDR
0:02:28
BSI Medical Devices | Mapping Regulations IVDR
1:18:46
ESHG IVDR Webinar: Section 2 - IVDR – Impact on a diagnostic laboratory
0:02:45
MDR and IVDR – The evolving challenges of EU regulations
0:00:16
In Vitro Diagnostic Device Regulation (IVDR)
0:04:45
BSI Compliance Navigator | MDR and IVDR – Key changes
1:27:25
ESHG IVDR Webinar: Section 3 - IVDR - Obtain regulatory compliance for IH-IVD’s
0:32:44
What are the new rules for In-Vitro Diagnostic Industry with IVDR 2017/746?
0:01:01
Understanding the MDR & IVDR: What Medical Device Companies Need to Know.
0:02:42
Identifying if a product is an IVD under EU IVDR 2017/746
0:59:59
Your Journey to IVDR Certification – A Roadmap to 2022
0:01:54
BSI Medical Devices | IVDR Timeline
0:03:13
What Are The New EU IVDR Regulations & How Are They Different To IVDD?
0:51:23
IVDR Checklist for Obtaining CE Marking & Maintaining EU Market Access
0:01:25
Was oder wofür ist die IVDR?
0:38:18
How to become the Best PRRC Ever? [EU MDR & IVDR]
0:31:06
European and national implementation of the IVDR
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