The Canadian product registration process is considered a licensing process that not only sources, but uses US-FDA submission requirements. This innovative product clearance process is efficient, but at the same time needs to be understood in order to avoid costly clearance delays.
 
 
GEMAR's expertise in registering medical products in Canada ensures an effective and efficient product registration experience. In addition, we remain in close contact with Health Canada to ensure effective management of these dynamic, ever-changing processes.