NUCRO-TECHNICS is a Pharmaceutical Contract Research Organization (CRO) that is a partner to pharmaceutical, biologic, and medical device companies located all over the world.  In business since 1970, we are located in a state-of-the-art 60,000 square foot facility a short drive from downtown Toronto, Canada.  Employing a staff of more than 170 scientific support personnel, our analysts have more than 4,000 years of combined experience with significant expertise in testing both large molecule and small molecule compounds.  As an organization Nucro-Technics is inspected by, and is in compliance with:

  • The US FDA (Food and Drug Administration);
  • Health Canada;
  • The Standards Council of Canada to the OECD GLP Standard; and
  • ISO 9001:2015

Our vision is to make our clients happy by providing excellent quality and service in all that we do.


Not just a CRO, Nucro-Technics’ capabilities clearly distinguish us as a full service Pharmaceutical Contract Support Organization – with qualifications and experience significantly different from those organizations that provide only testing services.  We work with a wide array of partners that range from small virtual companies looking to fulfill GLP IND requirements, to Fortune 500 companies looking to meet their GMP product release and stability testing obligations.  Not only does Nucro-Technics routinely complete projects for the 10 biggest pharmaceutical companies in the world, but we also provide analytical support to regulatory agencies, trade associations, and consultants looking to meet both GMP and GLP requirements.

Let’s Work Together
For further information about these services, a complete list of services available, to receive a quotation, schedule a test, or if there is something specific that you require, get in touch.