Prof. Bawazir Pharma Consulting Center offers various training programs for pharmaceutical professionals. Here are some of the training programs they provide:
Regulatory Affairs Training
– Basics of Drug Regulatory Affairs SFDA System Explained Training: This training program provides an explanation of the SFDA system and regulatory requirements, beneficial for professionals working in scientific offices, regulatory affairs, and pharmaceutical manufacturers.
– Advance Regulatory Understanding SFDA Drug Pricing System, Reimbursement and Market Access: This training covers SFDA’s pricing policy, reimbursement, and market access, providing insights into regulatory requirements and industry best practices.
Pricing System Explained
The training on the pricing system provides an in-depth understanding of the regulatory framework governing drug pricing in Saudi Arabia. Participants will gain insights into the SFDA’s pricing policy, including the factors that influence pricing decisions, reimbursement mechanisms, and market access strategies. This training is beneficial for professionals involved in pricing, market access, and regulatory affairs.
Chemistry, Manufacturing, and Controls (CMC) Training
The CMC training program provides a comprehensive understanding of the CMC section of the Common Technical Document (CTD). Participants will learn about the requirements for CMC documentation, including the development and manufacture of active pharmaceutical ingredients (APIs) and finished products. This training is beneficial for professionals involved in product development, manufacturing, and quality control.
Pharmacovigilance Training
– Comprehensive SFDA Pharmacovigilance System Explained Basic and Intermediate: This training program provides a comprehensive understanding of pharmacovigilance principles, SFDA regulations, and industry best practices.
– Advance Comprehensive Pharmacovigilance Training: This advanced training program covers topics such as signal detection, risk management, and pharmacovigilance system maintenance.
Good Manufacturing Practice (GMP) Training
– Basic of Good Manufacturing Practice (GMP) SFDA Explained: This training program provides an explanation of SFDA GMP guidelines and how to prepare for inspections.
– Advance GMP I Oral Solid Dosage Form: This training covers GMP principles for oral solid dosage forms, beneficial for professionals working in product development, technology transfer, and quality operations.
– Advance GMP II Sterile Medicinal Products: This training program covers GMP principles for sterile medicinal products.
Common Technical Documents (CTD) and eCTD Preparation Training
– Common Technical Documents (CTD) and (eCTD) preparation: This training program provides insights into compiling eCTDs, sharing best practices, and explaining the eCTD review and lifecycle process.