結果 : eu medical device regulatory affairs conference
58:56

The New EU MDR PMS Requirements Webinar

NSF
4,426 回視聴 - 5 年前
3:31:37

EMA webinar on Article 117 of the Medical Devices Regulation EU 2017/745

European Medicines Agency
5,380 回視聴 - 3 年前
49:50

Current Challenges in MDR (Medical Device Regulation) in the EU - Webinar with NO-FEAR Project

PerSys Medical
1,324 回視聴 - 3 年前
8:01

The future of medical device regulation in the European Union – EuroPCR 2019

PCR
795 回視聴 - 5 年前
34:10

MedTech Summit 2020 | EU Medical Device Regulation, Notified Body Overview and Update from BSI

BSI Group
2,034 回視聴 - 3 年前
2:14

Enhancing Regulatory Affairs in the Market Placing of New Medical Devices: the impact of AI

Artificial Intelligence - ing. Fabio Di Bello
16 回視聴 - 1 か月前
1:06:28

Medical Devices Regulation Training

MedTechEurope
35,280 回視聴 - 6 年前
17:30

Obtaining Regulatory Approvals for Medical Devices in a Global Market

IBF - International Business Forum
1,183 回視聴 - 12 年前
1:01:42

EU Medical Device Regulation: Your Questions Answered

Premier Research
677 回視聴 - 5 年前
1:53:18

Workshop on Good Regulatory Practices and its implementation in the Medical Device Sector 11/08/22

IAC Regulatory Convergence MedTech
27 回視聴 - 2 年前
1:00:39

European Medical Device Regulation - Recent Highlights and Status

Association of Graduate Regulatory Educators
2 回視聴 - 2 年前
3:31

Regulators Discuss New EU Regulations at TCT2016

Informa Content & Media Support
32 回視聴 - 7 年前
26:05

What did we learn about the EU Medical Device Situation at Medtech Forum?

Easy Medical Device
738 回視聴 - 2 年前
24:51

ISO 14971:2019 State of the Art, Standard of Care | Michelle Lott at 10x Medical Device Conference

MedicalMarcom
1,969 回視聴 - 4 年前
32:34

Medical Device News, Septembre 2024 Regulatory Update

Easy Medical Device
773 回視聴 - 1 か月前
21:12

Medical Devices and the Artificial Intelligence Act

Medical Device Regulatory Affairs by MeddiQuest
124 回視聴 - 3 年前
18:34

Active Implantable Medical Devices under the EU MDR - with Notified Body BSI

Informa Connect Life Sciences
1,564 回視聴 - 3 年前
57:26

Best Practices to Write a EU MDR Clinical Evaluation Report (CER) - A Webinar Video SARACASolutions

Saraca Solutions
2,440 回視聴 - 4 年前
36:18

Meet the Authors, Global Medical Device Regulatory Strategy, Second Edition

Regulatory Affairs Professionals Society
93 回視聴 - 3 年前

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1:06:05

Regulatory Affairs

Industry Pharmacists
43,771 回視聴 - 4 年前