Note: All training programs require physical presence and will be held in Riyadh at Bawazir Pharma Center
| FEES | SAUDI RIYAL |
| REGISTRATION FEES | SAR 2000.00 |
EARLY BIRDS REGISTRATION FEE
PAY YOUR FEE BEFORE 12 March, 2023. |
SAR 1000.00 |
OVERVIEW
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.
Download Brochure Basics of Good Manufacturing Practice (GMP) SFDA Explained 13 March 2023
LEARNING OBJECTIVES
At the conclusion of this training, participants will be able to:
- Understand the principals of SFDA GMP guidelines.
- Describe the different types of GMP inspection.
- Understand The general GMP inspection components
KEY TOPICS
- GMP Legal Framework
- Type of GMP Inspection
- Quality Management
- Personnel
- Premises and Equipment
- Documentation
- Production
- Quality Control
- Contract Manufacture and Analysis
- Complaints and Product Recall
- Self Inspection
WHO WILL ATTEND
Professionals working in:
- Pharma Regulatory Affairs
- Fresh Graduate
- Scientific Office Managers
- Regulatory Authorities.
- Pharmaceutical manufacturers
- Pharmacist
- CRO staff