Medical Devices Regulation (MDR)
Are you facing challenges in complying with MDR requirements?
At NAALA, we understand your concerns and are here to help. We specialize in addressing these challenges and ensuring that you can meet and maintain compliance with the MDR requirements. Our expertise lies in guiding businesses like yours through the complex regulatory landscape. We provide you with the necessary strategies and solutions to overcome these challenges and ensure a seamless compliance process.
Quality Officer as a Service
MDR & ISO 13485 implementation
Qualification and classification analysis
Internal audits and audit preparations
Internal audit
Quality Officer as a Service
MDR & ISO 13485 implementation
Qualification and classification analysis
Internal audits and audit preparations
2023
Software as a Medical Device manufacturer - 2023
Software as a Medical Device manufacturer - 2023
Software as a Medical Device manufacturer - 2023
Software as a Medical Device manufacturer - 2023
Software as a Medical Device manufacturer - 2023
Pharmaceutical wholesaler - 2023
Medical Device manufacturer - 2022/2023
Software as a Medical Device manufacturer - 2023
Software as a Medical Device manufacturer - 2023
Software as a Medical Device manufacturer - 2022/2023
Several Medical Device manufacturers - 2022/2023
Software as a Medical Device manufacturer - 2022/2023
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