The Food and Drugs Act (FDA) provides the regulatory requirements for the registration and sale of drug products in Canada. Q&R Canada Inc. offers a full range of regulatory affairs services for drug products ranging from submissions to continuous GMP compliance.

Regulatory Affairs

Whether you require us to spearhead the process or review documentation prepared by your company, Q&R is able to successfully achieve regulatory drug approvals from Health Canada.

  • New Drug Submissions or New Drug Applications with Health Canada
  • Submission expertise through to NDS/NDA drug approval in Canada

GMP Quality and Control

We will manage all aspects of your licensing process: Application, Inspection and Post-approval GMP compliance.

Rely on Q&R Canada as your trusted partner for Canadian Regulatory Compliance. Working with you as your regulatory partner, we can and will provide exceptional, personalized and expert service as an integral component in building and protecting your company’s brand and profits.