SFDA – RIAR Consulting

SFDA: Saudi Food and Drug Authority

Introduction

End-to-end SFDA regulatory expertise for confident market entry

Riar Consulting provides end-to-end regulatory consulting services for companies seeking market entry and compliance with the Saudi Food and Drug Authority (SFDA).

We support manufacturers and distributors across medical devices, IVDs, cosmetics, and other regulated products by aligning technical documentation, regulatory strategy, and submission execution with current SFDA regulations and guidance documents.

Our SFDA team focuses on precision, proper classification, correct application structuring, and proactive query management—ensuring efficient approvals and long-term compliance

OUR EXPERTISE – SFDA

How We Support SFDA Compliance

We assist clients across the full SFDA regulatory lifecycle, including:

Product classification and regulatory pathway assessment
SFDA Product Classification System (PCS) submissions
Medical Device Marketing Authorization (MDMA) applications
Authorized Representative (AR) agreement support
Importation and Distribution License (MDIL) applications
UDI registration in SAUDI-D
Cosmetics registration via eCOSMA
Renewals, updates, and variations
Regulatory query handling and authority communication

Each project is handled through a structured workflow aligned with SFDA’s Medical Device Regulations (MDS), guidance documents, and technical requirements.

WHY RIAR FOR SFDA

Why Choose Riar Consulting for SFDA

Strong understanding of SFDA device bundling and classification rules
Practical experience handling complex, multi-device portfolios
Focus on reducing unnecessary applications and rework
Clear documentation mapping aligned with SFDA folder structures
High approval success rate through compliant strategy
Dedicated SFDA regulatory consultants managing each submission

Our approach minimizes delays, avoids rejection risks, and improves regulatory predictability.

WHO LEADS – SFDA

Dedicated expertise ensuring compliant SFDA approvals

Each SFDA project is led by a dedicated regulatory consultant with hands-on experience in SFDA medical device and cosmetic registrations.

The lead consultant oversees:

Regulatory strategy and application structuring
Document review and gap assessment
Submission execution and follow-ups
Client communication and progress reporting

This ensures accountability, clarity, and consistent quality throughout the project lifecycle.

Vision 2030

Simplifying SFDA Compliance With Expert Precision

Let’s collaborate to shape a future where opportunities are limitless.

RIAR Consulting is a global regulatory consulting firm supporting medical devices, IVDs, cosmetics, and regulated products across key markets.

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(+91)99 274 94539

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info@riarconsulting.in

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7/38 Savitri Nagar Colony,New Jhunsi, Prayagraj, UP, 211019

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RIAR Consulting Private Limited