ABOUT US

The National Inherited Bleeding Disorder Genotyping Laboratory was founded in 2000 to provide molecular diagnostic testing for hemophilia A, hemophilia B, von Willebrand disease, and rare bleeding disorders.

 

The laboratory is supported by the Association of Hemophilia Clinic Directors of Canada, and by the Queen’s University Department of Pathology and Molecular Medicine. 

 

Tests may only be ordered by care givers from Canadian hemophilia comprehensive care centers and from clinical genetics clinics across Canada.

 

The lab is licenced by the Ministry of Health and Long-term Care (MOHLTC) to provide molecular diagnostics for hemophilia A, hemophilia B and von Willebrand disease. 

 

 

The lab is accredited by the Institute for Quality Management in Healthcare (IQMH) to ISO 15189. 

WHO WE ARE

Laboratory Director: Dr. David Lillicrap, MD FRCPC

 

Laboratory Co-Director: Dr. Paula James, MD FRCPC

Medical Laboratory Technologist: Gina Jones, MLT

Senior Medical Genetics Technician: Shawn Tinlin, VT

Medical Genetics Technician: Aomei Mo

Medical Genetics Technician: Christine Brown

Senior Clinical Scientist: Dr. Laura Swystun, PhD

Senior Clinical Scientist: Dr. Orla Rawley, PhD

DATA PRIVACY AND ACCESS TO INFORMATION

The NIBDGL is committed to ensuring the privacy and confidentiality of all collected information in accordance with all legal requirements.  For any inquiries into the NIBDGL’s information practices, please contact us at NIBDGL@queensu.ca. To obtain access to your report, please contact your referring clinician.