INTRODUCTION
Good Distribution Practice (GDP) is the part of quality assurance which ensures that products are consistently stored, transported and handled under suitable condition as required by the marketing authorisation (MA) or product specification.
PROGRAMME OBJECTIVES
- Discuss the development of the rules and guidelines of GDP
- Investigate the implications
- Potential risks to product safety and the control systems in place within their organization.
WHO SHOULD ATTEND?
- Managers
- Supervisors
- Personnel involved in storage and distribution
- Anyone who has responsibility for finished pharmaceutical products, intermediates or raw materials during storage and distribution – including transportation
PROGRAM OUTLINE
- Instruction
- Rationale & Development
- Legislation
- Provision of information to Authorities
- Organisation, Personnel & Responsibilities
- Management & licence holders
- Responsible Person
- Warehousing & Distribution
- Facilities & Equipment
- The Receipt
- The Storage
- Self-Inspection
- Documentation
- Orders
- Procedures
- Records
- Distribution
- Transportation
- Complaints & Returns
- Recalls
- Destruction
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