Overview:
Mapping and evaluating all the steps in a pharmaceutical manufacturing and packaging workflow can lead to valuable process improvements
Why you should Attend:
This course will describe the basic elements of pharmaceutical manufacturing and packaging and give you the tools that can help you develop a new workflow or improve upon an existing workflow.
- Describe general information related to the manufacture of finished pharmaceuticals and packaging
- Outline the factors to keep in mind when manufacturing certain drug types (e.g., penicillin)
- Describe the parameters of laboratory testing and Quality Assurance acceptance or rejection of batches
- Articulate the types of errors that can occur within the manufacturing and packaging workflows
- Investigate and determine root cause(s) for errors and design corrective and preventive actions (CAPAs)
- Articulate the requirements for transfer of product to warehousing and distribution
- Review workflows once created and documented to achieve process improvements
Areas Covered in the Session:
- Overview of finished product manufacturing
- Importance of packaging in the finished product process
- In-house verification methods (e.g., bar codes)
- Laboratory testing and possible product defects
- Finished product batch review and approval/rejection
- Packaging and distribution of finished product
- Considerations related to product intermediates
- Labeling and transfer of finished product to warehousing and distribution
Who Will Benefit:
- This course will be of benefit to Employees who are tasked with creating New Manufacturing Workflows or Revising Existing Workflows for Finished Product and Packaging