تفاصيل الدورة
Introduction to the concept GCP, GLP and GCLP- History
- The scope of application
- Benefits
- Trial Facility Management Responsibilities
- Analytical Project Manager Responsibilities
- Trial Staff Responsibilities
- Trial Facilities
- Archive Facilities
- Waste Disposal
- Equipment
- Material
- Reagents
- Receipt
- Chain of Custody
- Logistics
- Development and review of standard operating procedures
- Application of Standard Operating Procedures
- Analytical Plan
- Content of the Analytical Plan
- General
- Computer Systems
- Method Validation
- Processing trial materials
- General
- Analytical Report
- Content of the Analytical Report
- Analytical results
- Quality Control
- Quality Audit
- Storage and Retention of Records
- Confidentiality
المتطلبات
Qualified participants must be reasonably proficient in English to understand and fulfill the training requirements
الموقع
Medical Auditing and Quality أسئلة ذات صلة
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