0:31
NSF Webinar on the Life Science Sector in Ireland: Promo
NSF
37:15
Changing Requirements for Manufacturers Under IVDR
1:30
Why Work at NSF?
42:08
Enrichment Strategies to Increase the Power Reduce the Sample Size in Clinical Trials
1:55:13
Seminário On-line: Requisitos Internacionais para Fabricantes de IVD
59:45
Regulatory Q&A Session With NSF Experts
14:47
Adopting Digital Solutions in the Medical Device Industry
1:42
Are You Prepared for MDR/IVDR?
28:50
Webinar: A Regulatory Q&A With IVD Expert Robyn Meurant
3:06
EU MDR Training by NSF International
0:16
NSF's Remediation Resources
57:13
Reopening your business and the use of face masks
41:18
Emergency Market Authorization for COVID-19 IVDs. Emergency Use Authorization (EUA)
32:55
Upgrading the FDA Adverse Event Reporting Systems - FAERS
51:27
Webinar: Clinical Investigations - Transitioning from MDD to MDR
50:28
Clinical Evidence for Medical Devices Under Regulation (EU) 2017/745
1:21
How to meet new European Reg. Requirements for IVDs
47:54
How to Deal With the New Post-Market Surveillance Requirements Under Regulation (EU) 2017/745
39:39
Clinical Evidence for Medical Devices
International Standard for Medical Device Quality Management Systems
Medical Device Complaint Handling
In Vitro Diagnostic Device Regulation (IVDR)
31:43
Implementing a Simplification Strategy | NSF International
0:25
How to prepare for EU MDR
58:56
The New EU MDR PMS Requirements Webinar
LIVE
[Private video]
2:36
Medical Device Regulation Training - MDSAP Training
1:03:12
How to prepare for the changes to OEM medical devices under the new MDR
35:15
In Vitro Diagnostic Regulation - IVDR
42:39
Future of Clinical Data and Medical Device Regulation 2017/745
28:51
MDSAP - Medical Devices Single Audit Program Training
7:03
NSF Medical Devices Services
