Drug Regulatory Affairs

Drug Regulatory Affairs is the function that prepare submissions for approval by Health Canada to conduct clinical trials and to market new prescription medicines in Canada. Once these medicines are marketed, Drug Regulatory Affairs is responsible to maintain these products in compliance with the Health Canada requirements. Extensive interactions with colleagues in various part of the companies both locally and globally are necessary. Individuals in this function are well organized with good time management and communication skills. A university degree in a biological science or related field is necessary.