Profile

The Post-Diploma Certificate in GxP of Quality Assurance & Compliance (QAC) (PDC2 of Specialist Diploma in Biomedical & Pharmaceutical Engineering) aims to train the learners on the following:

Apply Good Laboratory Practices (GLP) in laboratory management in compliance to regulatory requirements.
Evaluate Corrective Action/Preventive Active (CAPA) and Quality Risk Assessment (QRM) in compliance to regulatory requirements.
Manage internal quality audit according to regulatory requirements at workplace.

What You'll Learn

The Post-Diploma Certificate in GxP of Quality Assurance & Compliance (QAC) (PDC2 of Specialist Diploma in Biomedical & Pharmaceutical Engineering) covers the following modules (total 150hrs):

GLP@Laboratory
Industrial Safety & WSHA
CAPA & Risk Assessment
Integrated-Work-Study Project in Quality Assurance & Compliance
Regulatory Compliance & ISO 13485
Lab Management & ISO 17025

Elective Modules (select 2)

Quality Risk Management
Medical Device Design & Validation
GLP Audit Management

Minimum Entry Requirement

The admission requirements for public intake are:

Candidates should have a recognised university degree or polytechnic diploma in engineering or science or other relevant disciplines.
Candidates with degrees or diplomas in other (non-relevant) disciplines, who have relevant work experience (RWE) will be considered.
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.