Quality Check! BAAT has successfully passed the ISO 13485 recertification audit by our Notified Body MedCert with ZERO non-conformities! Why does this matter for you? Navigating MDR compliance (EU Medical Device Regulations) is one of the toughest challenges for Medtech startups. When partnering with BAAT’s MDR-compliant processes, you gain: ➜ A faster path to market, reducing costly delays ➜ Confidence in a robust ISO 13485 Quality Management System ➜ Support for seamless regulatory compliance in the Medtech sector BAAT’s solutions are tailored for Medtech innovators. We help you focus on scaling your business while we handle the complexities of compliance. Ready to accelerate your Medtech journey? Visit us at www.baatmedical.com! #MDR #ISO13485 #MedTech #RegulatoryCompliance #Startups
Consistency is the key. Bravo :)
UPDATE: our Regulatory Expert Jasper Springer spotted a Non Conformity in our post above. Of course the stamp should be ISO 13485 (and not ISO 13845).