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Curricular information is subject to change
On completion of the module students should be able to:
1. Outline industry regulations and guidelines relating to C&Q
2. Describe key manufacturing technologies used in the biopharmaceutical industry
3. Interpret design documents required for the generation of installation and functional tests
4. Equipment/instrument receipt verification
5. Impact/risk assessments
1. Outline industry regulations and guidelines relating to Commissioning &Qualification (CQ)
2. Describe key manufacturing technologies used in the Biopharma Industry
3. Interpret design documents required for the generation of installation and functional tests of equipment required for biomanufacturing
4. Equipment/instrument receipt verification
5. Impact/risk assessments
Student Effort Type | Hours |
---|---|
Autonomous Student Learning | 104 |
Lectures | 16 |
Total | 120 |
Not applicable to this module.
Description | Timing | Component Scale | % of Final Grade | ||
---|---|---|---|---|---|
Continuous Assessment: Details of assignments will be provided at the start of the trimester | Varies over the Trimester | n/a | Graded | No | 100 |
Resit In | Terminal Exam |
---|---|
Summer | No |
• Feedback individually to students, post-assessment
Feedback can be requested by emailing the module teacher.
Name | Role |
---|---|
Padraig Williams | Lecturer / Co-Lecturer |