+46(0) 70 58 60 200 info@medqtech.com Follow us

Contact Us Today
To Connect With
Our Medical Device
Regulatory And
Quality Experts

Extend your team effectively, engaging regulatory compliance and quality into your business

 
 

Comply
Effectively
with


MDR 2017/745


IVDR
2017/746


ISO
13485


ISO
14971


QSR
(FDA)


CE-marking process

Our medical device customers are based right across the Nordics and beyond.

 

To get started we would recommend a consultative led open discussion about your medical device business goals.

Our customer partnerships and relationships are important to our business values. Todays video and screen sharing technology enables efficiency and opportunity to help medical device organizations with quality and regulatory compliance across the globe.

If your medical device company wants to enhance and accelerate its regulatory compliance journey or roll out a quality management system, please do not hesitate in
contacting us.

Request a meeting /information

 

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    West Coast office:

     

    T: +46(0) 70 58 60 200
    E: info@medqtech.com

    MedQtech, Rörviksvägen 40A
    457 95 Grebbestad, Sweden

     

    East Coast office:

     

    MedQtech,
    KontorEtt
    Köpmangatan 1
    852 31 Sundsvall, Sweden

    “To get our innovational medical device to market we needed a partner to advise us and help us to achieve regulatory compliance efficiently. The MedQtech team has been excellent, advising us on classification and regulation needs, taking us through the quality journey, including implementing an eQMS - we could not have asked for more.”

     

    Medical device company