The healthcare industry is changing and we have the breadth of expertise to help you evolve with it.
Comprehensive service offerings at every point in the product life cycle.
Our software tools offer digital regulatory monitoring for medical device compliance and access to human factors engineering tools.
The latest industry news and insights from our global team.
Stay informed with the most read RA/QA medical device newsletter.
TalkingPoints is a round-up of news, insights, and resources about human factors and usability for medical devices, IVDs, combination products, and more.
Information and tools to advance your business.
Learn from our experts through live events.
Our global consulting team works from 20+ offices on six continents.
Performance Evaluation – When, What and How to Prepare for EU IVDR (Presented in Portuguese)
Este webinar explica o conceito de Avaliação de Desempenho apresentado pelo IVDR 2017/746 e aspectos fundamentais a considerar para seu produto.
MDR: Common Issues for Medical Device Manufacturers (Presented in Portuguese)
This presentation, presented in Portuguese, reviews the resources of the European Commission.