Headquartered in Toronto, Canada, PharmEng Technology is a full service consulting firm that serves the pharmaceutical, medical devices and biotechnology industries in North America and internationally. Since 1997, the company has provided industry recognized consulting services assisting clients in the rapid commercialization of new product from drug discovery, strategic planning to process scale up. PharmEng business covers:

• Analytical Development
• Formulation Development
• Validation and Scale up
• Regulatory Audits and Compliance
• Engineering
• Quality Systems Development and Audits
• GMP Audits, SOP development
• Medical Devices
• Investigative testing (clinical trials)
• Medical device product licenses and establishment licenses
• Mandatory problem reporting
• Certified Training in pharmaceutical and biotechnology industry

PharmEng stays current with regulatory changes in the USA, Canada and Europe to ensure that it meets a truly upfront global perspective. With over 100 full-time professionals, it now has offices operating in Ontario, British Columbia, Nova Scotia, Manitoba, USA, and Asia. Current clients, many being multinational, are from North America, Asian-pacific, Europe and Africa representing the pharmaceutical, biotechnology and medical devices industries.