Human Factors Engineering is an essential part of medical product development and has progressively become a major focus of regulators over the last decade, most notably the US FDA. This seminar will cover an introduction to the discipline, an overview of the current regulatory expectations and examples of lessons learned illustrated by real-world case studies and is provided free of charge by medHF, a provider of Human Factors Engineering services to many of the world’s leading medical device and pharmaceutical companies.

Program

To attend the event you can contact the email thiago.figueiredo@med-hf.com

Time: 10 am - 12 pm
Venue: Barcelona Science Park · Edifici Torres R+D+I · C/ Baldiri Reixac, 4-8
Language: English