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Latest Articles

  • Saudi Drug Information (SFDA SDI)

    Drug Information and Stock Reporting to SFDA (SDI)

  • PSSF in SFDA

    Saudi PV Sub System (PSSF)

  • SFDA recall procedure in Saudi Arabia

    Product Recall in Saudi Arabia

  • SDEA-Requirements-by-SFDA

    SDEA Agreement Requirements by SFDA

  • The registration timelines in SFDA for all types of products.

    SFDA Timelines

  • What are the reference countries in SFDA?

    SFDA Reference Countries

  • How to submit a safety report ICSR to SFDA

    ICSRs Submission to SFDA

  • Signal Management Workshop (March 2023 Riyadh)

  • How to submit a PSUR to SFDA and what are the requirments?

    PSUR: SFDA requirements

  • The new route of registration for low risk medical device

    SFDA Cancels the MDNR Procedure

  • Medicinal gas registration in Saudi as a medical device

    Medical Gas Registration

  • Product label and artwork requirements in Saudi Arabia according to SFDA.

    SFDA Labelling Requirements

  • Clinical trials CRO requirements

    SFDA Clinical Trials Requirements in Saudi Arabia

  • Food Supplements Registration in Saudi Arabia (SFDA)

    Food Supplements Registration

  • NDLP: Saudi Pharmaceutical Market is expected at $11.7 billion by 2030 (Views on Medical Devices Included)

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