Good Maintenance Practices in pharmaceutical industries
Engineering and Validation
Operations
Quality
- Duration
- 3 days (2 days can be customized)
- Course fee
- -
Program Description
Topics to be covered with this training includes:
|
Target Level
- Validation and Qualification scientists, Supervisor and Manager
- Engineering Department Staff (Maintenance, Project Management, Utilities Engineers)
- Professionals from service organizations and vendors who serve pharmaceutical clients
- Quality Department (QA and Compliance)
- Regulatory bodies involved in pharmaceutical industries
- Internal/External Auditors and consultant
- Production Manager or supervisors
Description
Objectives and Expected Results
- Participants will take Idea on how to differentiate between different type of maintenance
- Participants will take the idea of how to connect the maintenance activities with the sustainability of process and quality of the product
- Participants will able to plan for the maintenance program and share all relevant departments
- Participants will take an idea about the best maintenance practice and how it effects on system reliability and efficiency
- Participants will take Idea about GMP aspects that are correlated with maintenance
- Participants will take an idea about the handling of maintenance proprieties and differentiate between maintenance based on the impact of the product
- Participants will be able to harmonize international regulation versus fieldwork
Others Training Materials
Workshop, Sheets and case studies paper will be conducted and implemented during training
Target group
-
-
Trainer Languages English/Arabic
Sign up
Interested in signing up a group of people for this course?
Please contact our Business Development team:
[email protected]
00962 798756232