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Featured Articles

  • Types of products registration in SFDA (Saudi Arabia)

    SFDA Registration and Approval Process

  • SFDA Medical Device Registration (MDMA)

  • How to register a drug in Saudi Arabia (SFDA)

    SFDA Drug Registration Requirements

  • Learn about pharmacovigilance and QPPV requirements by SFDA in Saudi Arabia

    Pharmacovigilance & QPPV Requirements in Saudi Arabia

  • orphan drug in Saudi Arabia

    Orphan Drug Designation (ODD) in SFDA

  • SFDA expedited pathways & drug designations

    Expedited SFDA Pathways and Drug Designations

Latest Articles

  • SFDA Patent Rules for Generic Drugs

    Saudi Genric Drug Patent Regulations (SFDA FTO)

  • SFDA incentive list to register shortage drugs

    What Is the SFDA Drug Incentive List? Types and Hidden Benefits

  • SFDA expedited pathways & drug designations

    Expedited SFDA Pathways and Drug Designations

  • How to Register Borderline Products in the SFDA?

  • eCTD Requirements SFDA

    What are the eCTD Requirements in SFDA?

  • PharmaKnowl at the Global Health Exhibition 2025

  • Exhibiting at the World Drug Safety Congress, Amesterdam 2025

  • We are exhibiting in the 24th ISoP Annual Meeting, in Cairo

  • Medical Device Establishment License (MDEL) in SFDA

    Medical Device Establishment License (MDEL)

  • SFDA preclinical study submission process in Saudi Arabia

    Preclinical Studies Submissions to SFDA

  • Step-by-step SFDA Drug Master File submission and approval process

    Drug Master File (DMF) & Letter of Access for SFDA

  • Overview of SFDA-accepted economic activities linked to commercial records for regulatory operations

    Commercial Record Economic Activities Accepted by SFDA

  • Illustration of Literature-Based Submission in SFDA

    Literature-Based Submissions in SFDA

  • Biowaiver under SFDA Guidelines for pharmaceutical product registration in Saudi Arabia

    Biowaiver Under SFDA Guidelines

  • SFDA drug renewal in Saudi Arabia

    SFDA Drug Renewal Process in KSA

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