Pharmaceutical Quality Assurance and Quality Control Diploma Program (includes practical laboratory work)

The Diploma in Pharmaceutical Quality Control and Quality Assurance (Dip.QCQA) provides students with the comprehensive knowledge and skills in the fields of Pharmaceutical Analysis, Quality Assurance and Regulatory Affairs. The courses are delivered by experts from both pharmaceutical and biopharmaceutical industries, using state-of-the-art technologies, to provide the students with strong technical and practical skills needed in a US-FDA and Canadian TPD regulated work environment.

The Diploma Program is delivered in three phases over a period of 12 months. Highlights of the courses delivered during the different phases are given below:

Diploma in Pharmaceutical Quality Assurance & Quality
Control Program

Introduction to Good Manufacturing Practices – Level I

Introduction to Pharmaceutical Laboratory Testing – Level I

Workplace Hazardous Material Information Systems (WHMIS)

Introduction to Pharmaceutical Dissolution Testing – Level I

Introduction to High Performance Liquid Chromatography – Level I

Introduction to Pharmaceutical Manufacturing Methods

Good Manufacturing Practices – Level II

Pharmaceutical Laboratory Testing – Level II

Pharmaceutical Dissolution Testing – Level II

High Performance Liquid Chromatography – Level II

Introduction to Pharmaceutical, Biological/Biotechnology, Natural Health Products and Medicines

Introduction to International Food and Drug Laws, Regulations and Guidelines

Technical Writing and Scientific Communication

Good Manufacturing Practices – Level III

Pharmaceutical Laboratory Testing – Level III

High Performance Liquid Chromatography – Level III

Regulatory Submission

Global Regulatory Strategies

Introduction to Auditing – level I

Advanced Auditing – Level II

Preclinical –Drug

Clinical – Drug

Cleaning Validation

Pharmaceutical Stability Program

Advance High Performance Liquid Chromatography – Level IV

Introduction to Clinical Trials

Chemistry Manufacturing and Control

Post Approval Activities and Compliance

Formularies and Reimbursement

Natural Health Products

Biologics/Biotechnology Products

Medical Devices

Labeling and Product Summaries

  • Document Reviewer
  • Laboratory Analyst
  • Laboratory Chemist
  • Validation Chemist
  • Stability Chemist
  • Laboratory Technician
  • QC Analyst
  • Document Control
  • QA Associate
  • QA Assistant
  • Manufacturing Auditor
  • Quality Auditor
  • Regulatory Affairs Associate
  • Regulatory Affairs Assistant
  • Project Coordinator
  • Manufacturing Specialist