Training activity information
Details
Distribute a product
Complete the required documentation and evaluate the recall process
Suggest improvements where appropriate
Type
Developmental training activity (DTA)
Evidence requirements
Evidence the activity has been undertaken by the trainee​.
Reflection on the activity at one or more time points after the event including learning from the activity and/or areas of the trainees practice for development.
An action plan to implement learning and/or to address skills or knowledge gaps identified.
Considerations
- Regulatory and good practice guidance
- Criticality of appropriate storage and distribution including cold chain
- Impact of recall process on patient safety
- Documentation
- Recall process
- Regulatory frameworks
- Cold chain
- Stock management
- Storage requirements
- Patient needs
Relevant learning outcomes
| # | Outcome |
|---|---|
| # 1 |
Outcome
Describe the working practices of pharmaceutical production. |
| # 3 |
Outcome
Perform a range of manufacturing activities, using specialist equipment, in accordance with requirements for GMP and pharmaceutical quality management systems. |
| # 5 |
Outcome
Perform activities to support safe storage and distribution of medicinal products applying the principles of Good Distribution Practice (GDP). |
| # 6 |
Outcome
Apply the principles of quality risk management to the manufacturing process. |