Toronto Institute of Pharmaceutical Technology (TIPT)
TIPT is North America's leading institute for pharmaceutical education and training, established in 1992. It offers practical programs and certifications in pharmaceutical manufacturing, research & development, quality assurance & quality control, regulatory affairs, high performance liquid chromatography, and quality control analyst certification. TIPT aims to equip students with industry-relevant skills through hands-on training, co-op placements, and state-of-the-art facilities, preparing them for successful careers in the pharmaceutical industry. The institute emphasizes the importance of documentation skills, GMP compliance, and scalable manufacturing processes, preparing students for various roles in pharmaceutical R&D, manufacturing, and regulatory environments.
Industries
Nr. of Employees
small (1-50)
Toronto Institute of Pharmaceutical Technology (TIPT)
Patents
Products
Pharmaceutical Manufacturing Technology diploma
52‑week diploma combining theoretical modules with hands-on GMP manufacturing training and an integrated co-op.
Pharmaceutical Research & Development diploma
52‑week diploma focused on theoretical and practical skills for drug development, including hands-on projects in GMP facilities.
Pharmaceutical Quality Assurance & Quality Control diploma
46‑week program covering QA/QC systems, sampling plans, laboratory testing and auditing practices, with co-op placement.
Pharmaceutical Regulatory Affairs diploma
40‑week diploma teaching regulatory approval pathways, application preparation and communication with regulatory authorities, including practical submission exercises.
High Performance Liquid Chromatography certificate
8‑week intensive certificate focused on HPLC instrumentation, method development and validation for analytical laboratories.
Pharmaceutical Quality Control Analyst Certificate
29‑week analyst certificate combining applied chemistry with practical pharmaceutical drug analysis training for candidates with prior laboratory experience.
Pharmaceutical Manufacturing Technology diploma
52‑week diploma combining theoretical modules with hands-on GMP manufacturing training and an integrated co-op.
Pharmaceutical Research & Development diploma
52‑week diploma focused on theoretical and practical skills for drug development, including hands-on projects in GMP facilities.
Pharmaceutical Quality Assurance & Quality Control diploma
46‑week program covering QA/QC systems, sampling plans, laboratory testing and auditing practices, with co-op placement.
Pharmaceutical Regulatory Affairs diploma
40‑week diploma teaching regulatory approval pathways, application preparation and communication with regulatory authorities, including practical submission exercises.
High Performance Liquid Chromatography certificate
8‑week intensive certificate focused on HPLC instrumentation, method development and validation for analytical laboratories.
Pharmaceutical Quality Control Analyst Certificate
29‑week analyst certificate combining applied chemistry with practical pharmaceutical drug analysis training for candidates with prior laboratory experience.
Services
Structured diploma programs combining theoretical instruction with hands-on training and integrated co-op placements across manufacturing, R&D, QA/QC and regulatory affairs.
Short intensive certificate focused on HPLC instrumentation, method development, troubleshooting and validation for pharmaceutical quality laboratories.
Program teaching QA/QC systems, sampling plans, audits, CAPA, change control and other compliance practices used in pharmaceutical and related industries.
Program covering regulatory approval processes, application types, change control and lifecycle regulatory documentation, with practical experience on real submissions.
Placement of students into industry work terms to gain practical experience with real pharmaceutical processes and submissions.
Online portal for domestic and international applicants to submit program applications and pay application fees.
Structured diploma programs combining theoretical instruction with hands-on training and integrated co-op placements across manufacturing, R&D, QA/QC and regulatory affairs.
Short intensive certificate focused on HPLC instrumentation, method development, troubleshooting and validation for pharmaceutical quality laboratories.
Program teaching QA/QC systems, sampling plans, audits, CAPA, change control and other compliance practices used in pharmaceutical and related industries.
Program covering regulatory approval processes, application types, change control and lifecycle regulatory documentation, with practical experience on real submissions.
Placement of students into industry work terms to gain practical experience with real pharmaceutical processes and submissions.
Online portal for domestic and international applicants to submit program applications and pay application fees.
Expertise Areas
- Pharmaceutical manufacturing operations
- Pharmaceutical research and development
- Quality assurance and quality control
- Regulatory affairs and submissions
Key Technologies
- High-performance liquid chromatography (HPLC)
- Gas chromatography (GC)
- Spectroscopy
- Analytical method validation
News & Updates
TIPT’s R&D team produced treatments for a groundbreaking HIV study on iron supplementation for children with HIV, published in The Lancet.
Insight into the relationship between pharmaceutical training and medical cannabis, highlighting practical skills and industry relevance.
An overview of Good Manufacturing Practices (GMP) and their importance in ensuring drug safety, efficacy, and quality.
TIPT’s research & development team were asked to produce treatments for a groundbreaking HIV study on the safety and efficacy of iron supplementation for children living with HIV, published in The Lancet.
Insight into the relationship between pharmaceutical training and medical cannabis, highlighting practical skills and industry relevance.
An overview of Good Manufacturing Practices (GMP) and their importance in ensuring drug safety, efficacy, and quality.
TIPT’s R&D team produced treatments for a groundbreaking HIV study on iron supplementation for children with HIV, published in The Lancet.
Insight into the relationship between pharmaceutical training and medical cannabis, highlighting practical skills and industry relevance.
An overview of Good Manufacturing Practices (GMP) and their importance in ensuring drug safety, efficacy, and quality.
TIPT’s research & development team were asked to produce treatments for a groundbreaking HIV study on the safety and efficacy of iron supplementation for children living with HIV, published in The Lancet.
Insight into the relationship between pharmaceutical training and medical cannabis, highlighting practical skills and industry relevance.
An overview of Good Manufacturing Practices (GMP) and their importance in ensuring drug safety, efficacy, and quality.