We are pleased to update that Aran now offers comprehensive human factors engineering services, complying with FDA guidance and international standards.
Our unique team of usability specialists, industrial designers, and regulatory experts apply human factors engineering throughout the development process to prevent use errors and speed up development.
We provide all required documentation related to usability, including formative testing, summative validations and the final usability report for submission.
To learn more about human factors engineering in medical devices and our services please contact:
Haya Belkind-Shafir | Human Factors Engineering Lead
ARAN Research and Development (1982)
EMAIL | haya.belkind@aran-rd.com MOBILE | +972 52 6508383
TEL | +972 4 623 9000 FAX | +972 4 627 32 60
