Learning Outcomes:
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
Indicative Module Content:
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