Home→Quality & Accreditations→Certifications, Accreditations & Licences

Quality begins with compliance

At Beauty Roots, we comply with the regulatory requirements in force in the Kingdom of Saudi Arabia and work with manufacturers and brands qualified to recognised quality and safety standards, to ensure the supply of reliable medical products to healthcare facilities.

01 Licences & regulatory compliance

Regulatory compliance at every stage

We operate in accordance with the requirements of the Saudi Food and Drug Authority, from product registration and import through to storage and distribution, while maintaining the documents and data needed for traceability and review.

SFDA

Saudi Food & Drug Authority

Compliance with the regulatory requirements governing the registration, import and distribution of medical products within the Kingdom.

Medical devices distribution licence: IDL-2024-MD-0095 Cosmetics storage & distribution licence: SWL-2024-CM-0262

02 Quality certifications & accreditations

Standards that support trust

Our supply system is built on working with qualified manufacturers, with due regard to the standards and accreditations relating to manufacturing systems, medical-device quality and product conformity.

GMP

Good Manufacturing Practice.

ISO 13485

Quality management system for medical devices.

The European conformity mark.

MDSAP

Medical Device Single Audit Program.

03 Brand & product accreditations

Brands we choose with care

We work with brands and manufacturers specialising in medical and aesthetic products, and review the technical and regulatory documents for each product against the requirements for distribution in the Kingdom.

ReMedium

Accreditation marks are shown as published on the brand's official website.

SCPN Cosmetic product notification
GMP Good Manufacturing Practice
ISO 13485 Medical device quality management
CE European conformity
US FDA US Food & Drug Administration
MDSAP Medical Device Single Audit Program
MFDS Korean MFDS approval
CPNP EU Cosmetic Products Notification Portal
SCPN Cosmetic product notification
GMP Good Manufacturing Practice
ISO 13485 Medical device quality management
CE European conformity
US FDA US Food & Drug Administration
MDSAP Medical Device Single Audit Program
MFDS Korean MFDS approval
CPNP EU Cosmetic Products Notification Portal
SCPN Cosmetic product notification
GMP Good Manufacturing Practice
ISO 13485 Medical device quality management
CE European conformity
US FDA US Food & Drug Administration
MDSAP Medical Device Single Audit Program
MFDS Korean MFDS approval
CPNP EU Cosmetic Products Notification Portal
SCPN Cosmetic product notification
GMP Good Manufacturing Practice
ISO 13485 Medical device quality management
CE European conformity
US FDA US Food & Drug Administration
MDSAP Medical Device Single Audit Program
MFDS Korean MFDS approval
CPNP EU Cosmetic Products Notification Portal

HA Filler

The conformity and registration marks relevant to the product are shown once they have been matched against the official documents.

Pending document verification

Hairont · GynWell · OVDs

Verified product accreditations are shown, with the accreditations of the manufacturer, Jingjia Medical, listed separately from those of the products.

Hairont Pending document verification

GynWell Pending document verification

OVDs Pending document verification

Manufacturer approvals

Jingjia Medical

Manufacturer of HA Filler, Hairont, GynWell and OVDs. These approvals cover the manufacturer itself, not each individual product.

ISO 13485Medical device quality management
ISO 9001Quality management system
MDSAPSingle audit program

04 Regulatory documents

Documentation available when needed

We provide medical facilities with the technical and regulatory documents relating to our products, as approved and made available by the manufacturers, to support their review and procurement procedures.

Documents available per product

Technical product information Instructions for use Relevant registration and accreditation documents

Request documents