ورش عمل

Showing 76–80 of 80 results

  • Pharmaceuticals Pricing, Reimbursement and Market Access. SFDA System Explained 14 September, 2021 Riyadh

    The rise in costs of pharmaceutical products in general affects all sectors of the health care industry, including private insurers and patients. This workshop shall give an overview on the pricing practices of pharmaceutical products in SFDA and GCC_DR. In addition, a thorough discussion on the pricing policy by SFDA shall be presented and what you need to learn to price your products.

    2,000.00 SAR
    Details
    Registration

  • Pharmaceuticals Pricing, Reimbursement and Market Access. SFDA System Explained 22 June, 2022 Riyadh

    The rise in costs of pharmaceutical products in general affects all sectors of the health care industry, including private insurers and patients. This workshop shall give an overview on the pricing practices of pharmaceutical products in SFDA and GCC_DR. In addition, a thorough discussion on the pricing policy by SFDA shall be presented and what you need to learn to price your products.

    2,000.00 SAR
    Details
    Registration

  • Post Approval Activities and Compliance: Variations Guideline 15 March, 2021 Riyadh

    This course will provide an overview and analysis of the various regulatory activities that take place post-approval: In particular, the current regulatory climate will be discussed in depth and numerous examples will be provided to illustrate effective filing of notification techniques. Common issues which have caused difficulties for pharmaceutical firms will also be discussed.  The training will discuss in detail the GCC guideline for variations management and post approval commitment.

    1,500.00 SAR
    Details
    Registration
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    Preparing VNeeS Submission 11 April, 2021 Riyadh

    This course will offer insight into the compilation of the VNees, share experience and best practices gained during VNees  submissions to SFDA.

    • Overview of VNees readiness at the agencies
    • Impact of the VNees on regulatory processes and procedures
    • VNees compilation and life cycle management
    • VNees Validation
    • Document granularity and readiness
    • Technical issues
    • Specifications and standards

    1,500.00 SAR
    Details
    Registration

  • Preparing VNeeS Submission 31 March, 2021 Riyadh

    This course will offer insight into the compilation of the VNees, share experience and best practices gained during VNees  submissions to SFDA.

    • Overview of VNees readiness at the agencies
    • Impact of the VNees on regulatory processes and procedures
    • VNees compilation and life cycle management
    • VNees Validation
    • Document granularity and readiness
    • Technical issues
    • Specifications and standards

    2,000.00 SAR
    Details
    Registration
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