Regulatory affairs - United States medical devices
Regulatory affairs - Europe pharma
Regulatory affairs - Europe biologicals
Regulatory affairs - Europe nutraceuticals
Regulatory affairs - Europe medical devices
Regulatory affairs - global markets
Validation
Headquartered in Toronto, Canada, PharmEng is a full-service consulting and contract manufacturing company that serves the pharmaceutical, biotechnology and medical device industries in North America and internationally.
PharmEng’s consulting focus is to provide engineering, validation, regulatory affairs and regulatory compliance solutions for their clients in the pharmaceutical and biotechnology sectors. With the expansion into contract manufacturing, the company now offers a complete service to assist clients in the rapid commercialization of new products from strategic planning to process scale up and final production.
Canadian consulting offices are located in Vancouver, Winnipeg, and Toronto with USA operations in Durham (NC), San Francisco (CA), Boston (MA), Atlanta (GA), Philadelphia (PA) and Princeton (NJ). International operations include Beijing (China) and Taipei (Taiwan). Manufacturing facilities are located in Perth, Ontario with a new 46,400 sq. ft. facility in Cape Breton, Nova Scotia.
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 consulting professionals, clients are multinational corporations from North America, Asian-pacific, Europe and Africa representing the pharmaceutical, medical devices and bio-technology industries.
