How to use Harmonized Standards for Medical Devices?
What Are Harmonized Standards Under EU MDR And EU IVDR?
Webinar 'Harmonized Healthcare Standards' - part 1.
Complying with Standards - Medical Device Basics
What's going on with the harmonization of regulatory standards across geographies?
Harmonisation of African Standards on Pharmaceuticals and Medical Devices
CE Marking - What does it mean?
Harmonized Standards
Why you need ISO 13485 for your medical device manufacturing project
Which external standards should be referenced in a submission?
Webinar for standard drafters - The DOs and DONTs of drafting medical device harmonised standards
Webinar 'Harmonized Healthcare Standards' - part 2.
Embedded Software in Medical Device : Common Regulatory and Quality pitfalls
EU Medical Device Regulation (MDR) Takes Full Effect on May 26, 2021
IS ISO 13485 A HARMONIZED STANDARD?
MDR Series: TIPS with ISA. Tip 1: Finding and Use of Harmonized Standards in EU MDR Regulation.
Overview of EU regulations for in-vitro Diagnostic Medical Devices
Labeling Requirements for Medical Devices in Europe
Medical Device News, Septembre 2024 Regulatory Update
IVD Technical File Compilation
Changes in Europe’s Medical Device Regulations: Consequences for Manufacturers
The European Medical Device New Regulation 2017/745
IVDR Checklist for Obtaining CE Marking & Maintaining EU Market Access
E-Lecture Series / Daniel Rubisoier: Regulatory requirements for medical devices
Webinar Inclusive standards: European Commission’s study on Anthropometrics in harmonized standards
What are EN standards in the European Union?
Medical Device News - August 2021 Regulatory Update [MDR & IVDR]
Active Medical Devices in Europe: Particular Requirements
Webinar: Development of harmonised standards under the MDD/MDR
Webinar (Feb 2017) Postmarket Compliance ISO 134852016 & New European Medical Device Regulations
MDR with Brexit, how the combination is impacting the European medical device industry.
Update to European harmonised standards
Medical Devices: Managing Evolving Standards in Multiple Jurisdictions
How to build a winning strategy for EU MDR Compliance & Medical Device Regulatory requirements
The Harmonized Standard: Myths, Legends, And Its Growing Role In The Marketplace, recorded 8/9/18
Regulatory Framework for Medical Devices & Iv-Vitro Diagnosis Part 2
Enhancing Exports to Europe for Medical Devices - Legislations & Certifications
MedTech Summit 2020 | EU Medical Device Regulation, Notified Body Overview and Update from BSI
CE Marking Around the World: How to Enhance the Achievements of the CE Marking to Open More Markets
Medical Device News - March 2020 Regulatory Review (EU MDR)
Medical Devices Webinar by Asphalion
VLOG | MDR is Here - Now What?
BIS Talks on Standardization of Medical devices
Week 5.4 CE certification for medical device
Criticality of Medical Device Risk Management for Patient and Product Safety
Building a Technical File - Brandwood Biomedical Webinar
The 5 most relevant changes the Medical Device Regulation MDR introduces, that you must know
European Medical Device Registration Chapter 3 - Quality Management System
TGA Webinar: Regulation of Software As a Medical Device
Medical Device Usability: Highlights of European Regulations and the Latest Standards
TGA Webinar: Unique Device Identification #1
Regulatory Standards & Risk Management in Medical Devices
Basics of medical products regulatory harmonization
Notified Body Survey - Interesting statistics
Mexico Medical Device Market Access and ISO 13485 certification
Russia Medical Device Market Access, ISO 13485, and CE Marking for Medical Device Manufacturers
Webinar We're Off! Implementing the European MDR and IVDR with recordings
CEN and CENELEC workshop on Personal Protective Equipment – Medical Devices (MD) dual use products
REKOM BIOTECH implements the ISO 13485 standard
Medical Device News - December 2022 update
US FDA Standards Overview
FCI Clinical Safety SIG: What do the clinical safety standards and medical device requirements mean?
Medical Devices Regulation Training
Medical Device Regulation in a Post Brexit World
Understanding ISO 14971 2012
Preparing for the Radio Equipment Directive
COVID-X OC#1 Introduction into the medical device regulatory landscape. Part 1 - Webinar
Developing AI-Powered Medical Devices - Matrix Requirements Webinar
Medical Device News - May 2021 Update
Introduction to the GHTF or IMDRF
Medical Device News: February 2022 Regulatory Update
SVP Packaging - NB Persepective on CE-marked Medical Devices-Article 117 MDR Combination Products
Introduction to CE Marking (April 2014)
EMA webinar on Article 117 of the Medical Devices Regulation EU 2017/745
Medical Device News: July 2022 Regulatory update
: BSI-AAMI International Standards & Regulations Conference - Day 1
Interactive Q&A Nov 2021- Medical Device Cybersecurity (Nov 2021)
CORE-MD Webinar: The Origins and objectives of the European Medical Device Regulation
2020-02 -2 Regulatory Requirements for Active MedTech
Clinical Evidence for Medical Devices
ISO 14971:2019 & TR 24971 Explained - Medical Device Risk Management
The ABCs of Medical Device Software Compliance under EU Regulations 2017/745 and 2017/746 - Webinar
2018 Medical Device Regulation EU 2017/745 Training v1.0
The value of the ISO 14155 standard for clinical investigations
Ultimate guide to placing a medical device on the EU market
Connected Medical Devices
An introductory guide to medical device Clinical Evaluation & Clinical Evaluation Reports (CER)
Bristows reacts: the future regulation of medical devices in the UK
MDR Effects on Processing Devices
Medical Packaging Regulatory & Standards Update (March 31, 2020)
6 - Compton - Standards-Setting in the Context of Regulatory Harmonization
Regulatory tips for medical device and IVD developers
Regulatory Q&A Session With NSF Experts
ISO 14971 : 2019 ( Medical Device Risk management ) | Detailed explanation Clause by Clause
Unlocking the British and European markets with UKCA and CE marking
Free webinar on Medical Devices Regulation - MDR & MDSAP
WHAT IS THE PRIMARY OBJECTIVE OF ISO 13485?
Clinical Evidence for Medical Devices Under Regulation (EU) 2017/745
(Medical Device) Third Party Certification- PMDA-ATC Learning Videos
SIEMIC News - EU Commission Revises R&TTE Directive Harmonized Standards Listing
