NAALA | Not An Average Legal Advisor

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.

Related capabilities

Quality Officer as a Service

MDR & ISO 13485 implementation

Qualification and classification analysis

Internal audits and audit preparations

Internal audit

Want to Do It Yourself?
Related capabilities

Quality Officer as a Service

MDR & ISO 13485 implementation

Qualification and classification analysis

Internal audits and audit preparations

Want to Do It Yourself?
Our recent cases

2023

QMS and Technical File Template package

Software as a Medical Device manufacturer - 2023

MDR implementation

Software as a Medical Device manufacturer - 2023

QMS and Technical File Template package

Software as a Medical Device manufacturer - 2023

MDR implementation

Software as a Medical Device manufacturer - 2023

Technical file writing

Software as a Medical Device manufacturer - 2023

Qualification and classification of MDSW

Pharmaceutical wholesaler - 2023

Quality Manager as a Service

Medical Device manufacturer - 2022/2023

ISO 13485 implementation

Software as a Medical Device manufacturer - 2023

Qualification and classification of MDSW

Software as a Medical Device manufacturer - 2023

Person Responsible for Regulatory Compliance

Software as a Medical Device manufacturer - 2022/2023

Internal audits

Several Medical Device manufacturers - 2022/2023

Quality Manager as a Service

Software as a Medical Device manufacturer - 2022/2023

Let us know what you are looking for and we will get back to you as soon as possible.

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