Medical Devices

Quality & Regulatory

Strategic, technical and regulatory services for medical device development

Specialised consulting services for medical devices companies

Our priority at MDQ Services Ltd is guaranteeing your success.

Whether you’re goals are:

• seeking to expand your operations;

• increase your technological performance;

• enhance your organisational effectiveness;

• achieve regulatory compliance.

We’re here to make sure that the process is well planned and executed.

Our team is experienced in a wide variety of business processes to make sure

you get the most professional results every time.

Services for your business

Discover our services as UKRP for Medical Devices

UK Responsible Person

Learn about services such as UKRP to market Medical Devices in the UK.

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Swiss Authorised Representative

Learn about services such as CH-REP to market Medical Devices in Switzerland.

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CE Marking

Learn about certification services for trade in the EU.

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DISCOVER OUR ADDITIONAL SERVICES

DISCOVER WHAT ELSE WE CAN DO FOR YOU

Complying with regulations is essential

It is critical to the timely launch of the device and future market growth that the regulatory aspects are developed in conjunction with the design, verification, and validation of the device itself.

All business stakeholders must work towards the same goal.

MDQ Services Ltd helps companies understand the current and foreseeable regulatory environment in Europe and the UK.

We also understand how regulations apply to specific devices, taking into account the development timelines and technical documentation for each type of regulation.

Find out how we can help your company.

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