About QnR Associates
QnR Associates was formed to support applicants and License Producers in the Marihuana for Medical Purposes industry. The principal consultants have extensive experience in Quality Assurance, Regulatory Affairs, Quality Control and Manufacturing in the Pharmaceutical, Biotechnology, Natural Health Product, Medical Device industries and Marihuana for Medical Purposes (ACMPR) industry. The group has supported many clients to establish GMP manufacturing within Canada, USA and other global countries.
The group also has experience in the import and export of products to and from many regulatory jurisdictions. Specialties include Quality Management (Quality Assurance), Product Review and Release, CMC (Chemistry, Manufacturing and Controls), Validation (Process, Equipment, Methods, Facilities), NDS (New Drug Submissions), IND/CTA, Process Mapping, Quality Control, Manufacturing, Product License Application, Facility Design, Site License Application, GMP, GCP, GLP, Investigations, Root Cause analysis and initiation and effectiveness monitoring of Corrective and Preventive Actions. The principals have significant experience in all stages from conception and design, to creation, implementation and ongoing management of these types of programs.