ورش عمل

Showing 46–60 of 81 results

  • Online Basic of Good Manufacturing Practice (GMP) SFDA Explained 9 June 2024 Riyadh

    Understanding basics of GMP are essential skills for people working in pharmaceutical industry. This course will provide an explanation to SFDA GMP guidelines and how to prepare for inspection. This training will also enhance understanding and be beneficial to persons who work in scientific offices, regulatory affairs, pharmaceutical manufacturers, data management, basic research, project management and marketing, etc.

    4,500.00 SAR
    Details
    Registration

  • Pharmaceuticals Pricing, Reimbursement and Market Access. SFDA System Explained 11 October, 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.

    2,500.00 SAR
    Details
    Registration

  • Pharmaceuticals Pricing, Reimbursement and Market Access. SFDA System Explained 11 January, 2023 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.

    2,500.00 SAR
    Details
    Registration

  • Post Approval Activities and Compliance: Variations Guideline 8 November, 2022 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.

    2,000.00 SAR
    Details
    Registration

  • Preparing VNeeS Submission 24 October, 2022 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

    2,500.00 SAR
    Details
    Registration

  • SFDA Pharmacovigilance System Explained 09-10 March, 2021 Riyadh

    Understanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, and marketing, etc.

    4,500.00 SAR
    Details
    Registration

  • SFDA Pharmacovigilance System Explained 1-2 March, 2022 Riyadh, Saudi Arabia

    Understanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, and marketing, etc.

    4,500.00 SAR
    Details
    Registration

  • SFDA Pharmacovigilance System Explained 13-14 June, 2023 Riyadh, Saudi Arabia

    Understanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, and marketing, etc.

    5,500.00 SAR
    Details
    Registration

  • SFDA Pharmacovigilance System Explained 15-16 February, 2021 Riyadh

    Understanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, and marketing, etc.

    4,500.00 SAR
    Details
    Registration

  • SFDA Pharmacovigilance System Explained 15-16 May, 2023 Riyadh, Saudi Arabia

    Understanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, and marketing, etc.

    5,500.00 SAR
    Details
    Registration

  • SFDA Pharmacovigilance System Explained 16-17 May, 2022 Riyadh, Saudi Arabia

    Understanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, and marketing, etc.

    4,500.00 SAR
    Details
    Registration

  • SFDA Pharmacovigilance System Explained 17-18 January, 2022 Riyadh

    Understanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, and marketing, etc.

    4,500.00 SAR
    Details
    Registration

  • SFDA Pharmacovigilance System Explained 19-20 March, 2023 Riyadh, Saudi Arabia

    Understanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, and marketing, etc.

    5,000.00 SAR
    Details
    Registration

  • SFDA Pharmacovigilance System Explained 22-23_August, 2023 Riyadh, Saudi Arabia

    Understanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, and marketing, etc.

    6,000.00 SAR
    Details
    Registration

  • SFDA Pharmacovigilance System Explained 23-24 November, 2021 Riyadh

    Understanding Pharmacovigilance System in Saudi Arabia is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working as Qualified Person of Pharmacovigilance (QPPV) in the regulatory affairs departments or related fields, who need knowledge of the SFDA Pharmacovigilance System and processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, and marketing, etc.

    4,500.00 SAR
    Details
    Registration
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