Aesthetic Quality Assurance Register

Join the Device-Link™ Aesthetic Quality Assurance Register

Demonstrate your commitment to patient safety, quality and regulatory excellence. AQAR is an independent digital register for manufacturers and distributors committed to the highest standards of product quality and post-market surveillance.

Quality Assured · Trusted · Transparent

AQAR — Quality, Safety, Transparency

Independent quality assurance for aesthetic products

Why AQAR exists

Regulatory excellence, made demonstrable

AQAR works in alignment with the objectives of the MHRA, JCCP and Healthcare Inspectorate Wales to support patient safety, promote the use of regulated aesthetic products, and help reduce the risks associated with unregulated products and procedures — supporting UK and EU regulatory requirements and professional body standards.

Differentiate your products in an increasingly competitive market with independent quality assurance and real-world evidence.
Strengthen post-market surveillance and build trust with clinics, practitioners and patients.
Show a verifiable, ongoing commitment to the highest standards of product quality and patient safety.

Benefits of registration

Go beyond registration. Demonstrate ongoing quality

Registration is more than a quality mark. It gives your organisation access to a digital post-market intelligence platform that strengthens compliance, generates real-world evidence, and builds confidence across the market.

Digital quality assurance badge

Display a verified digital badge across your website, marketing and product packaging to demonstrate your commitment to quality, transparency and patient safety.

Enhance practitioner confidence

Help clinics identify manufacturers committed to continuous quality monitoring and patient safety.

Improve customer engagement

Maintain an ongoing relationship with healthcare professionals and patients after distribution, rather than losing visibility once products enter clinical practice.

The Device-Link™ platform

Real-world evidence, from routine practice

Developed by industry experts in product safety and regulatory excellence, and used in the NHS, Device-Link™ provides a secure digital infrastructure that captures valuable real-world evidence directly from routine clinical practice — strengthening quality systems while supporting better patient outcomes.

Collecting high-quality post-market data across independent clinics is difficult: patient outcomes, practitioner feedback and adverse-event information are often fragmented across locations and systems. Device-Link™ brings them together.

PMS

Strengthen post-market surveillance

Collect real-world product performance data from healthcare professionals and patients to support ongoing PMS activities.

PMCF

Simplify clinical follow-up

Gather long-term clinical outcomes, patient satisfaction and safety information through secure digital follow-up.

Signals

Earlier detection of safety signals

Identify trends in adverse events, product performance and patient outcomes sooner, enabling faster investigation and corrective action.

RWE

Generate real-world evidence

Build a growing evidence base to support product performance, regulatory submissions, publications and commercial growth.

Audit

Support inspection readiness

Access dashboards and reports that demonstrate proactive post-market surveillance and continuous product improvement.

What's collected

Product name, manufacturer, CE and UKCA compliance data, UKRP, PMS and PMCF — with quality-of-life questionnaires and survey data feeding your evidence base.

Quality Assured · Trusted · Transparent

Become a recognised leader in aesthetic patient safety

Join the Device-Link™ Aesthetic Quality Assurance Register today and demonstrate your commitment to patient safety, regulatory excellence and continuous quality improvement.

Frequently asked

Questions, answered

What is the Device-Link™ Aesthetic Quality Assurance Register?

An independent register of verified products and their authorised manufacturers and distributors.

Who can join the register?

Manufacturers and distributors of aesthetic products.

How does Device-Link support post-market surveillance?

It captures product feedback, complaints and alerts through its app-based platform.

Is Device-Link suitable for UK MDR and EU MDR compliance?

Yes.

How is patient data protected?

Data is securely protected through encrypted infrastructure.

What information is collected?

Product name, manufacturer, CE and UKCA compliance data, UKRP, PMS and PMCF.

How does Device-Link help generate real-world evidence?

Through quality-of-life questionnaires, survey data and the capture of product feedback.

Contact us

We'd love to hear from you

Whether you have a question about AQAR, would like to register, explore partnership opportunities, or need support, send us a message and we'll respond as soon as possible.

  • Emailinfo@device-link.com
  • HoursMonday–Friday, 9:00am–5:00pm (UK)
  • ResponseWe aim to respond within 2 working days.
Loading form…