Industry Focus

The healthcare industry is changing and we have the breadth of expertise to help you evolve with it.

Overview
Doctor listening to baby's heart
Next
Previous
Services

Comprehensive service offerings at every point in the product life cycle.

Overview
RAMS®

A platform of digital products to improve, simplify and automate RA/QA activities

Learn more
OPUS™

Emergo by UL's new human factors tool - provides training, tools, and resources.

Learn more
Software

Our software tools offer digital regulatory monitoring for medical device compliance and access to human factors engineering tools.

Overview
News

The latest industry news and insights from our global team.

View all
RADAR : Market Access Newsletter

Stay informed with the most read RA/QA medical device newsletter.

Sign up
TalkingPoints : Human Factors Newsletter

TalkingPoints is a round-up of news, insights, and resources about human factors and usability for medical devices, IVDs, combination products, and more.

Sign up
Resources

Information and tools to advance your business.

View all
Events

Learn from our experts through live events.

View all
Doctor sitting at a desk taking notes from a labtop
Next
Previous
About

Our global consulting team works from 20+ offices on six continents.

Overview
global representation of the Earth
Next
Previous
  • On-demand Webinar

MDR: Common Issues for Medical Device Manufacturers (Presented in Portuguese)

In order to help manufacturers adjust to the new regulatory environment, Medical Devices Regulation 2017/745 established a number of new supporting documents and services.

Contact us
Folders, pen, and notepads on a table
THE CONTENT OF THIS WEBINAR IS FOR GENERAL INFORMATION PURPOSES ONLY AND IS NOT INTENDED TO CONVEY LEGAL OR OTHER PROFESSIONAL ADVICE.

Assista ao vídeo: RDM: Temas Comuns aos Fabricantes de Dispositivos Médicos

A fim de ajudar os fabricantes a se adaptarem ao novo ambiente regulatório, o Regulamento MDR 2017/745 para Dispositivos Médicos estabeleceu vários novos documentos e serviços de suporte.

Data do webinar 

29 de maio de 2023

Palestrante

Sarah Mundim, Consultora Senior RA/QA

Esta apresentação analisa os recursos da Comissão Europeia, tais como: 

  • Atualizações relevantes sobre o MDR desde junho de 2022 
  • Experiência da indústria de dispositivos médicos até o momento com o MDR 
  • Temas comuns nas revisões das submissões MDR pelos Organismos Notificados  
  • Discussão sobre os Documentos de Posicionamento do MDCG e Team NB 
  • Documentos orientativos do MDCG
Person at computer attending a webinar

Attend an upcoming webinar

Ready to elevate your industry IQ with insights and news from experts? Register for one of our upcoming events.

View upcoming webinars
X

Request more information from one of our specialists

Thanks for your interest in our products and services. Let's collect some information so we can connect you with the right person.