Quality Risk Management (part of the PDC2 of Specialist Diploma in Biomedical & Pharmaceutical Engineering)
About This Course
This is part of Post-Diploma Certicate in GxP GxP of Quality Assurance & Compliance (QAC) of Specialist Diploma in Biomedical & Pharmaceutical Engineering.
This module consists of 15 hours of training.
This elective* module offers a training duration of 15 hours.
*Elective Modules (select 2)
• Quality Risk Management (15 hours)
• Medical Device Design & Validation (15 hours)
• GLP Audit Management (15 hours)
What You'll Learn
Entry Requirements
The admission requirements for public intake are:
1. Candidates should have a recognised university degree or polytechnic diploma in engineering or science or other relevant disciplines.
2. Candidates with degrees or diplomas in other (non-relevant) disciplines, who have relevant work experience (RWE) will be considered.
3. applicants who do not meet the above entry requirements may be considered based on Recognition of Prior Learning (RPL) with evidence of at least 5 yeas of RWE; or supporting evidence of competency readiness. Suitable applicants who are shortlisted may have to go through an interview and/or entrance test(s). The Polytechnic reserves the right to shortlist and admit applicants.