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MedEnvoy Global @UC8-oiQBMrd_aV28mgVUzV5Q@youtube.com

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MedEnvoy, Global BV | Our Mission: Provide a minimally invas


58:41
MDR Technical Documentation Requirements | MDR and IVDR Compliance Webinar
00:57
New Zealand Sponsor: How MedEnvoy Supports Your Medical Device Market Entry
56:46
Economic Operators Under the MDR and IVDR | MDR and IVDR Compliance Webinar
46:32
Post Market Surveillance | MDR and IVDR Compliance Webinar
54:30
MDR QMS Notified Body Assessment | MDR and IVDR Compliance Webinar
08:41
The Role of the Regulatory Importer for UK-Based Manufacturers | MDR & IVDR Compliance
57:08
QMSR FDA Webinar | Navigating FDA Compliance and Defining Your QMSR Journey
01:07
Mexico Registration Holder: Streamline Your Medical Device Registration
56:42
Regulatory Importer Responsibilities & Best Practices
02:50
Navigating EU Regulations for Medical Devices & IVDs
01:26
Your Global Partner for Medical Device Regulatory Compliance
00:55
EUDAMED Registration: Register Your Medical Device or IVD for EU Compliance
06:33
SaMD Best Practices for Transitioning to MDR/IVDR
06:18
CE Marking: Navigating the Challenges Faced by Medical Device Manufacturers
02:31
Isavela's Transition to MDR : Technical Documentation with MedEnvoy
01:56
What You Need To Know About Medical Device Importer Labeling
04:15
Customer Success Stories: Economic Operator Streamlines Process for Medical Device/IVD Manufacturers
02:37
Consolidating Economic Operators in Europe: In-Country Representation & Importer Services | MedEnvoy
01:42
In-Country Representation for Medical Devices and IVDs in the EU, UK, and Switzerland
04:09
Why Medical Device and IVD Manufacturers Need a Regulatory Importer
07:44
Swiss Importer and CH-REP: What Manufacturers Need to Know
01:43
Why You Need an EU Medical Device Importer