Upcoming events and training

Webinar — New ISO 10993-1 in Practice: A 360° View of Biological Evaluation

A high-level discussion on ensuring compliance with ISO 10993-1:2025, the main challenges in Biological Evaluation and Chemical Characterization, and how to integrate the process into medical device development.

February 26, 2026 at 1:00 PM

Online — live

Who should attend: Regulatory affairs, quality and R&D professionals in medical devices

Registration closed

CGA Training — Good Manufacturing Practices (RDC 665) for Health Products

Practical training on the requirements of RDC 665/2022: QMS structure, mandatory documentation, qualification and validation, and preparation for ANVISA inspections.

Date to be defined

Belo Horizonte — MG, Brazil (date to be defined)

Who should attend: Quality, production and regulatory teams of health product manufacturers