Guidelines

Guidance on Saudi Food and Drug Authority Policy for Collection of Patient Experience Data (MDS-G018)

Guidance on Saudi Food and Drug Authority Policy for Engagement with Healthcare Practitioners (MDS-G017)

Guidance on Saudi Food and Drug Authority Policy for Engagement with Patients (MDS-G019)

Guidance on SFDA Requirements for Quality Assurance Programs for Radiation Emitting and Imaging Devices (MDS-G15)

Guidance on Software as a Medical Device

Guidance on Submission of Chemistry, Manufacturing, and Control (CMC) Information for Human Gene

Guidance on the development of IVDs for in-house use

Guidance on the Procedures for Licensing of Medical Devices and Supplies Establishments

Guidance to update the database of products in SDR

Guide for Investor to Obtain a Pharmaceutical Manufacturer License

Guide for Licensing Consulting Services Establishment

Guide for the Procedures of Issuing a Validity Certificate to Export Food Products_T[2]