The Pharmaceutical Research & Development diploma is a program that teaches the theoretical knowledge needed to assist in the development and creation of innovative drug products. Students will get to experience these processes as they complete practical projects in TIPT’s industry standard GMP facility.

One of the most unique aspects of our program is that students receive training not just within the industry standards but also in innovative drug development techniques at our GMP facilities.

The Quality Assurance & Quality Control diploma is a program that teaches how to develop, monitor, and oversee measures that assures control, reproducibility and reliability of manufacturing and testing processes. Students also learn how to conduct sampling and testing required to evaluate compliance of the manufactured products to compendial standards of safety and effectiveness.

One of the most unique aspects of our program is the fact that students not only train in a fully GMP complaint and Health Canada-licensed facility of the same standard as used in  industry, but also practice their skills by auditing real pharmaceutical products batch records.

The Pharmaceutical Regulatory Affairs diploma is a program that provides a practical understanding of the regulatory approval and communication processes involving pharmaceutical and biotechnology drugs as well as natural health products and medical devices.

One of the most unique aspects of our program is that students to apply and integrate their knowledge in a “real-world” work setting under TIPT’s IPE system, and receive practical experience with actual submissions that have been approved by regulatory authorities.

The High Performance Liquid Chromatography certificate is an intensive course in HPLC instrumentation, method development and validation. The training ensures the development of necessary skills to operate & troubleshoot equipment, and develop & validate test methods in a pharmaceutical quality laboratory.

One of the most unique aspects of our program is our hands-on approach that provides students with the opportunity to apply and integrate their knowledge in a “real-world” work setting within TIPT’s state-of-the-art HPLC facility, utilizing the same type of equipment encountered in a professional setting.

The Pharmaceutical Quality Control Analyst Certificate is a hands-on pharmaceutical analysts program that combines applied chemistry with specific in-depth training in pharmaceutical industry drug analysis. This program is suited for individuals with strong background in chemistry and who have had prior laboratory experience.

One of the most unique aspects of our program is that with a duration of just over half a year, students learn through intensive training modules, providing them with an excellent option to upgrade their current industry skillset and knowledge.