This course provides an overview of good manufacturing practices and describes the elements of a well-designed pharmaceutical facility. This will include quality, safety, utilities, basic equipment, automation, maintenance and processing.
Biomanufacturing and support personnel
- Quality
- Safety
- Utilities
- Facilities, Equipment, Sensors, Automation
- Maintenance
- BioManufacturing Process
- Upstream Process
- Downstream Process
- Final Operations
- Controlling Cos
Attendees who have completed this course should be able to:
- Explain the uniqueness of our industry, culture and history.
- Define basic current good manufacturing practices (cGMP) principles and purpose of validation.
- Identify ways that operator and environmental safety are controlled in a pharmaceutical facility.
- Define the key utilities used.
- Explain where types of contamination, where it comes from and how it is controlled in the process.
- Identify basic manufacturing equipment, process sensors and what a distributed control system does.
- Explain how maintenance is performed in a pharmaceutical process.
- Define purpose of the upstream, downstream, and final operation processes and be able to identify key operations within these processes.
- Identify key software used throughout the facility and how cost is controlled.
Delivered in-person in a classroom or lab setting.
Delivered online with a live instructor at a scheduled date and time.
This course provides an overview of good manufacturing practices and describes the elements of a well-designed pharmaceutical facility. This will include quality, safety, utilities, basic equipment, automation, maintenance and processing.
Biomanufacturing and support personnel
- Quality
- Safety
- Utilities
- Facilities, Equipment, Sensors, Automation
- Maintenance
- BioManufacturing Process
- Upstream Process
- Downstream Process
- Final Operations
- Controlling Cos
Attendees who have completed this course should be able to:
- Explain the uniqueness of our industry, culture and history.
- Define basic current good manufacturing practices (cGMP) principles and purpose of validation.
- Identify ways that operator and environmental safety are controlled in a pharmaceutical facility.
- Define the key utilities used.
- Explain where types of contamination, where it comes from and how it is controlled in the process.
- Identify basic manufacturing equipment, process sensors and what a distributed control system does.
- Explain how maintenance is performed in a pharmaceutical process.
- Define purpose of the upstream, downstream, and final operation processes and be able to identify key operations within these processes.
- Identify key software used throughout the facility and how cost is controlled.
Delivered in-person in a classroom or lab setting.
Delivered online with a live instructor at a scheduled date and time.