Prochains événements et formations

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.

26 février 2026 à 13:00

Online — live

Public concerné: Regulatory affairs, quality and R&D professionals in medical devices

Inscriptions closes

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 à définir

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

Public concerné: Quality, production and regulatory teams of health product manufacturers