Note: Online training program.
Link will be sent one day before the training day
| FEES | SAUDI RIYAL |
| REGISTRATION FEES | SAR 4500.00 |
EARLY BIRDS REGISTRATION FEE
PAY YOUR FEE BEFORE 5 June 2024. |
SAR 2500.00 |
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.
Online
Download Brochure Online Basics of Good Manufacturing Practice (GMP) SFDA Explained 9 June 2024
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