Webinar: Understanding The Regulatory Landscape Of Drug-Device Combination Products In The Eu

Webinar: Understanding the Regulatory Landscape of Drug-Device Combination Products in the EU

NSF

DIA 2018: Navigating the Regulatory Landscape of Drug-Device Combination Products

DIA

Introduction to Drug-Device Combination Regulations in Europe

WMDO

Combination Products: Seeking Notified Body Opinion According to Article 117 - Webinar

Drug-Device combination products - Article 117 of EU MDR with Theresa Jeary

Easy Medical Device

Why should drug-device combination manufacturers know the different regulations in the USA and EU?

GCP-Mindset - All About Clinical Research

Understanding Regulation (EU) 2017/745, Article 117 for Combination Devices

SGS North America

Drug Device Combination Products | Episode 01- What are the Regulations for Combination Products?

Understanding Europe's Medical Device Regulation

Trends and Challenges in US and EU Combination Product Landscapes

Drug device combination products Lise Vanderkelen

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

European Medicines Agency

Drug Device Combination Products | Episode 03-Regulatory Procedure:Combination Products in EU Part-1

Drug Device Combination Products | Episode 05 -Notified Body Opinion in EU: Essential Steps (Part3)

Medical Devices Regulations Webinar - 24 January 2023

The New EU MDR PMS Requirements Webinar

NSF

Medical devices: regulations and chemical characterisation

Chemistry World

FDA PMSR Drug Device Combination Implementation Guide

TransCelerate BioPharma

Combination products: regulatory approach and cGMP requirements

Drug Device Combination products certificate for medical devices

Operon Strategist