ورش عمل
Showing 16–30 of 80 results
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Basics of Drug Regulatory Affairs SFDA System Explained Training 13 September, 2021 Riyadh
1,500.00 SAR Registration -
Basics of Drug Regulatory Affairs SFDA System Explained Training 17 November, 2021 Riyadh
1,500.00 SAR Registration -
Basics of Drug Regulatory Affairs SFDA System Explained Training 22 February, 2021 Riyadh
1,500.00 SAR Registration -
Basics of Drug Regulatory Affairs SFDA System Explained Training 31 May, 2021 Riyadh
1,500.00 SAR Registration -
Basics of Drug Regulatory Affairs SFDA System Explained Training 9 February, 2022 Riyadh
1,500.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 10 January, 2023 Riyadh
2,500.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 10 June 2024 Riyadh
2,500.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 22 November 2023 Riyadh
2,500.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 24 February, 2021 Riyadh
2,000.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 25 October, 2022 Riyadh
2,500.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 30 May, 2022 Riyadh
2,000.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 9 March, 2022 Riyadh
2,000.00 SAR Registration -
Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate 14-15 November 2023 Riyadh, Saudi Arabia
6,000.00 SAR Registration -
Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate 16-17 April 2024 Riyadh, Saudi Arabia
6,000.00 SAR Registration -
Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate 19-20_September, 2023 Riyadh, Saudi Arabia
6,000.00 SAR Registration
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Basics of Drug Regulatory Affairs SFDA System Explained Training 13 September, 2021 Riyadh
Understanding drug regulatory affairs in the GCC region is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working in the regulatory affairs departments or related fields, who need knowledge of the SFDA and GCC regulatory processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, project management and marketing, etc.
1,500.00 SAR Registration -
Basics of Drug Regulatory Affairs SFDA System Explained Training 17 November, 2021 Riyadh
Understanding drug regulatory affairs in the GCC region is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working in the regulatory affairs departments or related fields, who need knowledge of the SFDA and GCC regulatory processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, project management and marketing, etc.
1,500.00 SAR Registration -
Basics of Drug Regulatory Affairs SFDA System Explained Training 22 February, 2021 Riyadh
Understanding drug regulatory affairs in the GCC region is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working in the regulatory affairs departments or related fields, who need knowledge of the SFDA and GCC regulatory processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, project management and marketing, etc.
1,500.00 SAR Registration -
Basics of Drug Regulatory Affairs SFDA System Explained Training 31 May, 2021 Riyadh
Understanding drug regulatory affairs in the GCC region is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working in the regulatory affairs departments or related fields, who need knowledge of the SFDA and GCC regulatory processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, project management and marketing, etc.
1,500.00 SAR Registration -
Basics of Drug Regulatory Affairs SFDA System Explained Training 9 February, 2022 Riyadh
Understanding drug regulatory affairs in the GCC region is very important for persons working in pharmaceutical sector in the region. This course is specifically designed for persons working in the regulatory affairs departments or related fields, who need knowledge of the SFDA and GCC regulatory processes. This training will also enhance understanding and be beneficial to persons who work in clinical research, data management, basic research, project management and marketing, etc.
1,500.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 10 January, 2023 Riyadh
This course will offer insight into the compilation of the eCTDs, share experience and best practices gained during eCTD submissions in the GCC, explain the eCTD review and lifecycle process and the upcoming eCTD requirements.
2,500.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 10 June 2024 Riyadh
This course will offer insight into the compilation of the eCTDs, share experience and best practices gained during eCTD submissions in the GCC, explain the eCTD review and lifecycle process and the upcoming eCTD requirements.
2,500.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 22 November 2023 Riyadh
This course will offer insight into the compilation of the eCTDs, share experience and best practices gained during eCTD submissions in the GCC, explain the eCTD review and lifecycle process and the upcoming eCTD requirements.
2,500.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 24 February, 2021 Riyadh
This course will offer insight into the compilation of the eCTDs, share experience and best practices gained during eCTD submissions in the GCC, explain the eCTD review and lifecycle process and the upcoming eCTD requirements.
2,000.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 25 October, 2022 Riyadh
This course will offer insight into the compilation of the eCTDs, share experience and best practices gained during eCTD submissions in the GCC, explain the eCTD review and lifecycle process and the upcoming eCTD requirements.
2,500.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 30 May, 2022 Riyadh
This course will offer insight into the compilation of the eCTDs, share experience and best practices gained during eCTD submissions in the GCC, explain the eCTD review and lifecycle process and the upcoming eCTD requirements.
2,000.00 SAR Registration -
Common Technical Documents (CTD) and (eCTD) preparation 9 March, 2022 Riyadh
This course will offer insight into the compilation of the eCTDs, share experience and best practices gained during eCTD submissions in the GCC, explain the eCTD review and lifecycle process and the upcoming eCTD requirements.
2,000.00 SAR Registration -
Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate 14-15 November 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 Registration -
Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate 16-17 April 2024 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 Registration -
Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate 19-20_September, 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 Registration