This diploma program provides student knowledge and hands-on skills of a pharmaceutical laboratory, CMP, CLP, USP and variety of analytical instruments HPLC, UV-Vis, FT-IR, Dissolution, GC, TLC etc.
Program Length
Practicum
Hands-on practice in college laboratory
Financial Aid
The diploma of pharmaceutical quality control program will provide student working knowledge of analytical instrumental techniques (HPLC, UV-Vis, FT-IR, GC and dissolution), computerized integrators and troubleshooting techniques, and how to use the US pharmacopeia and British Pharmacopoeia in detail. Also teaching students current Good Manufacturing Practices(cGMP), FDA and International Conference on Harmonization (ICH) guidelines, applicable standard operating procedures, analytical monographs, basic organic chemistry, analytical chemistry, Student will practice a variety of tests in the laboratory.
After finishing this course students will perform complex chemical and physical analysis on a wide range of pharmaceutical products in accordance with standards and established procedures.
Applicant must have a Grade 12 level or a university degree or a Science college diploma and demonstrated competency in English.
Our state of Arts laboratory allows students to practice with different instrument such as HPLC, UV, IR, Dissolution and wet chemistry.
The pharmaceuticals Quality Control program focuses on equipment and instrument analysis skills and experience training in the chemical industry, food industry, cosmetic industry and pharmaceutical industry. The students will apply for position after finishing this program in the fellow industry:
- Pharmaceutical companies(industries)
- Cosmetic industries
- Food product industries
- Chemical products manufacture
- Federal and provincial governments
- Medical and research laboratories
- Environmental Laboratory
- Natural health product companies
Program Consultation: For further information, email info@pharmamedical.ca or call the Program Coordinator at 416-821-4876 or 647-996-5876
























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