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The Toronto Institute of Pharmaceutical Technology (TIPT®) is a corporate education and training ally to major pharmaceutical companies in North America and world-wide. Through our dedicated professional and research faculty we conduct corporate needs assessment, develop customized training, and facilitate in-house personnel development in keeping with evolving technological and compliance requirements of the industry.
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Through education and training, TIPT® assures corporate personnel advancement as well as provides documented training and certification. Our customized corporate training typically range between one-day to five-day seminars and workshops and includes:
• GMP Training (Introductory and Advanced)
• GCP and GLP Training
• Manufacturing Technology (Introductory and Advanced)
• Formulation Technology
• Controlled Delivery Technology
• Regulatory Affairs & Drug Licensing
The advantage here is that the material is directly relevant and of immediate practical benefit to the company and employees. Customized programs can be delivered in-house (at your facility), off-site (at TIPT®’s facilities). Our commitment to excellence is reflected in the quality of our competent, certified graduates who utilize the education, training and experience gained through us for the advancement of the industry and society as a whole.
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Since it’s inception in 1992, TIPT® has successfully established corporate partnerships with leading pharmaceutical companies world-wide and has provided innovative product development solutions uniquely supported by pragmatic institutional experts.
Our Product Development and Corporate Services division offers cost-effective science-based drug development and GMP manufacturing services to the pharmaceutical, biopharmaceutical, natural products and allied industries in |
North America and world-wide.
TIPT® Pharmaceutical Product Development division provides the following services:
Biopharmaceutic Evaluation
of new and existing drug candidates to develop rationale for plausible routes of dosage administration and dosage form selection.
Preformulation
of potential drug candidates for feasible routes of administration, formulation composition, composition compatibility, and preliminary stability assessment.
Formulation Development
of new dosage forms or re-formulation of existing dosage forms using scientific design of experiment (DOE) and formulation technology to optimize selected formulation composition.
Our multi-disciplined expertise in pharmaceutical formulation, regulatory compliance, manufacturing technology, and biopharmaceutics has supported our proven ability to provide comprehensive product development solutions and services to our clients.
