SFDA Products Registration: Detials & Insights
Description of SFDA registration in Saudi Arabia for products and companies covering drug, health, herbal, medical devices, and veterinary products.
SFDA Stability Study Requirements
A summary of stability studies requirements in SFDA and GCC countries. What are the minimum time, zone, and the accepted commitments.
SFDA GMP: Manufacturer registration Process
Manufacturers have to comply with SFDA GMP requirements to be allowed to market in Saudi Arabia. Learn about that in this article.
SFDA Verification & Abridged Procedure for EMA/FDA approved applications
Learn about the requirements and timelines of the SFDA verification and abridged registration procedure.
Eligibility for SFDA Priority Review registration: 40% faster
Learn how to apply for SFDA priority review, what are the requirements and condition and how short is the reduced timelines?
SFDA Product Classification
Companies can apply for a product classification at the Saudi Food and Drug Authority (SFDA) based on the SFDA classification rules. The outcome of the classification confirms the following: Jurisdiction: whether it falls under the SFDA for registration and marketing regulation or a different Saudi authority. Acceptance for registration: some products are not allowed to …
Development of a Regulatory Strategy for the Saudi Market
Learn how to develop a regulatory strategy for your product registration in Saudi Arabia SFDA. What is the basic structure and the benefits.
SFDA Drug Registration: Requirements & Approval Process
Updated SFDA drug registration requirements and process description in Saudi Arabia. Guidelines, eCTD dossier, application, and fees.
What is SFDA Certificate?
Why you need an SFDA certificate and how you can secure it for your product. In this article you can learn about the SFDA approval document.