Prof. Bawazir Pharma Consulting Center

Common Technical Documents (CTD) and (eCTD) preparation
2026-04-09 09:00 - 16:00 (Europe/Moscow) | Bawazir Pharma Office, PJW5+79, Riyadh, 13513, Saudi Arabia
Date of training 9 April 2026 Riyadh Saudi Arabia

FEES
SAUDI RIYAL

REGISTRATION FEES
SAR 2900.00

EARLY BIRDS REGISTRATION FEE
PAY YOUR FEE BEFORE 7 April 2026.

SAR 2000.00

OVERVIEW
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.

Download Brochure Common Technical Documents (CTD) and (eCTD) preparation 9_April_2026 Riyadh

Basics of Drug Regulatory Affairs SFDA System Explained
2026-05-11 09:00 - 16:00
Date of training 11 May 2026 Riyadh Saudi Arabia

FEES
SAUDI RIYAL

REGISTRATION FEES
SAR 3400.00

EARLY BIRD REGISTRATION FEE
PAY YOUR FEE BEFORE 9 MAY 2026.

SAR 2400.00

OVERVIEW
Understanding drug regulatory affairs 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 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.
Download Brochure Basics of Drug Regulatory Affairs SFDA Explained 11 May 2026 Riyadh

Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate
2026-05-12 09:00 - 2026-05-13 16:00
Date of training 12-13 May 2026 Riyadh Saudi Arabia

FEES
SAUDI RIYAL

REGISTRATION FEES
SAR 6500.00

EARLY BIRDS REGISTRATION FEE
PAY YOUR FEE BEFORE 12 May 2026.

SAR 5200.00

OVERVIEW
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.

Download Brochure Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate_12-13 May_2026 Riyadh

Basics of Drug Regulatory Affairs SFDA System Explained
2026-07-06 09:00 - 16:30
Date of training 6 July 2026 Riyadh Saudi Arabia

FEES
SAUDI RIYAL

REGISTRATION FEES
SAR 3400.00

EARLY BIRD REGISTRATION FEE
PAY YOUR FEE BEFORE 5 July 2026.

SAR 2400.00

OVERVIEW
Understanding drug regulatory affairs 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 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.
Download Brochure Basics of Drug Regulatory Affairs SFDA Explained 6 July 2026 Riyadh

Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate
2026-07-07 09:00 - 2026-07-08 16:30
Date of training 7-8 July 2026 Riyadh Saudi Arabia

FEES
SAUDI RIYAL

REGISTRATION FEES
SAR 6500.00

EARLY BIRDS REGISTRATION FEE
PAY YOUR FEE BEFORE 5 July 2026.

SAR 5200.00

OVERVIEW
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.
Download Brochure Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate_7-8 July_2026 Riyadh

Basics of Drug Regulatory Affairs SFDA System Explained
2026-09-01 09:30 - 16:30
Date of training 1 September 2026 Riyadh Saudi Arabia

FEES
SAUDI RIYAL

REGISTRATION FEES
SAR 3400.00

EARLY BIRD REGISTRATION FEE
PAY YOUR FEE BEFORE 29 August 2026.

SAR 2400.00

OVERVIEW
Understanding drug regulatory affairs 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 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.
Download Brochure Basics of Drug Regulatory Affairs SFDA Explained 1 september 2026 Riyadh

Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate
2026-09-07 09:00 - 2026-09-08 16:30
Date of training 7-8 September 2026 Riyadh Saudi Arabia

FEES
SAUDI RIYAL

REGISTRATION FEES
SAR 6500.00

EARLY BIRDS REGISTRATION FEE
PAY YOUR FEE BEFORE 3 September 2026.

SAR 5200.00

OVERVIEW
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.
Download Brochure Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate_7-8 September_2026 Riyadh
