ServiceUpdated on 27 January 2025
FDA Rediness Audit
About
We have been in over 150 FDA audits of all types of devices globally and we know how to find the things that the FDA is looking for. Although the FDA is changing their qualty system regulation to adopt ISO 13485:2016, they attack from a differnt angle and we can help your organization get ahead of the curve before the change.
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Quality Management System Services for Medical Software
- Medtech
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Szabolcs Tóth, MBA
Regulatory Affairs and Quality Assurance Specialist for Medical Software at True North Consulting Kft.
Koroncó, Hungary
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Sara Ramió Pujol
Senior Regulatory Affairs Manager at Alira Health
Barcelona, Spain
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FDA Submissions including Documentation Preparation
Sara Ramió Pujol
Senior Regulatory Affairs Manager at Alira Health
Barcelona, Spain