ورش عمل
Showing 1–15 of 80 results
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Advance Comprehensive Pharmacovigilance Training 9-10 October 2023 Riyadh, Saudi Arabia
6,000.00 SAR Registration -
Advance GMP I Oral Solid Dosage Form 14 March 2023 Riyadh
2,000.00 SAR Registration -
Advance GMP I Oral Solid Dosage Form 2 November, 2022 Riyadh
2,000.00 SAR Registration -
Advance GMP II Sterile Medicinal Products 15 March 2023 Riyadh
2,000.00 SAR Registration -
Advance GMP II Sterile Medicinal Products 3 November, 2022 Riyadh
2,000.00 SAR Registration -
Advance Pharmacovigilance 05-06 April, 2021 Riyadh, Saudi Arabia
4,500.00 SAR Registration -
Advance Pharmacovigilance 19-20 October, 2021 Riyadh, Saudi Arabia
4,500.00 SAR Registration -
Advance Pharmacovigilance 24-25 May, 2022 Riyadh, Saudi Arabia
4,500.00 SAR Registration -
Advance Pharmacovigilance 3-4 October, 2022 Riyadh, Saudi Arabia
5,000.00 SAR Registration -
Advance Regulatory Understanding SFDA Drug Pricing System, Reimbursement and Market Access. 3 October, 2023 Riyadh
2,500.00 SAR Registration -
Basic of Good Manufacturing Practice (GMP) SFDA Explained 1 November, 2022 Riyadh
2,000.00 SAR Registration -
Sale!
Basic of Good Manufacturing Practice (GMP) SFDA Explained 13 March 2023 Riyadh
1,000.00 SAR Registration -
Basic of Good Manufacturing Practice (GMP) SFDA Explained 16 March, 2021 Riyadh
1,500.00 SAR Registration -
Basics of Drug Regulatory Affairs SFDA System Explained Training 10 January, 2022 Riyadh
1,500.00 SAR Registration -
Basics of Drug Regulatory Affairs SFDA System Explained Training 12 October, 2021 Riyadh
1,500.00 SAR Registration
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Advance Comprehensive Pharmacovigilance Training 9-10 October 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 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 -
Advance GMP I Oral Solid Dosage Form 14 March 2023 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 implementation. This training will also enhance understanding and be beneficial to persons who work in product development and Technology transfer, regulatory affairs, pharmaceutical manufacturers, production engineering, site engineering, project engineering, Quality Operations, facility support services etc.
2,000.00 SAR Registration -
Advance GMP I Oral Solid Dosage Form 2 November, 2022 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 implementation. This training will also enhance understanding and be beneficial to persons who work in product development and Technology transfer, regulatory affairs, pharmaceutical manufacturers, production engineering, site engineering, project engineering, Quality Operations, facility support services etc.
2,000.00 SAR Registration -
Advance GMP II Sterile Medicinal Products 15 March 2023 Riyadh
Understanding the Pharmaceutical Quality System is an essential skills for people working in pharmaceutical manufacturing industry. This course will provide an overview of the pharmaceutical quality system for sterile medicinal product as specified in SFDA GMP guidelines and prepare for implementation. This one day course is designed to increase their knowledge in contamination control strategy, specific technologies and will provide a comprehensive, yet practical assessment of the regulations. This training will also enhance understanding and beneficial to persons who work in product development and Technology transfer, regulatory compliance, pharmaceutical manufacturers, production engineering, site engineering, Quality Operations etc.
2,000.00 SAR Registration -
Advance GMP II Sterile Medicinal Products 3 November, 2022 Riyadh
Understanding the Pharmaceutical Quality System is an essential skills for people working in pharmaceutical manufacturing industry. This course will provide an overview of the pharmaceutical quality system for sterile medicinal product as specified in SFDA GMP guidelines and prepare for implementation. This one day course is designed to increase their knowledge in contamination control strategy, specific technologies and will provide a comprehensive, yet practical assessment of the regulations. This training will also enhance understanding and beneficial to persons who work in product development and Technology transfer, regulatory compliance, pharmaceutical manufacturers, production engineering, site engineering, Quality Operations etc.
2,000.00 SAR Registration -
Advance Pharmacovigilance 05-06 April, 2021 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 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 Registration -
Advance Pharmacovigilance 19-20 October, 2021 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 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 Registration -
Advance Pharmacovigilance 24-25 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 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 Registration -
Advance Pharmacovigilance 3-4 October, 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 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 Registration -
Advance Regulatory Understanding SFDA Drug Pricing System, Reimbursement and Market Access. 3 October, 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 Registration -
Basic of Good Manufacturing Practice (GMP) SFDA Explained 1 November, 2022 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.
2,000.00 SAR Registration -
Sale!
Basic of Good Manufacturing Practice (GMP) SFDA Explained 13 March 2023 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.
1,000.00 SAR Registration -
Basic of Good Manufacturing Practice (GMP) SFDA Explained 16 March, 2021 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.
1,500.00 SAR Registration -
Basics of Drug Regulatory Affairs SFDA System Explained Training 10 January, 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 -
Basics of Drug Regulatory Affairs SFDA System Explained Training 12 October, 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