medtech

As per ISO 13485, is it true or false that a medical device organization that uses spreadsheets is only required to validate spreadsheets that contain calculations?

Michelle Keane discusses CAPA in Medical Devices including potential reasons organizations struggle and the FDA raise so many findings in this area.

This insightful blog looks at the practicalities of performing a spreadsheet validation under ISO 13485.

Comply Guru proudly sponsored Global Access 2024 which is Ireland’s largest conference for Quality and Regulatory Affairs Professionals in Medical Devices.