Consultation: mandatory reporting of serious adverse drug reactions and medical device incidents

You’re invited to comment on proposed changes to the Food and Drug Regulations and Medical Devices Regulations. These changes would make it mandatory for health care institutions to report serious adverse drug reactions (ADRs) and medical device incidents (MDIs).

An Information Webinar on the consultation paper will be hosted by Health Canada on July 18.

If you are interested in attending the Information Webinar, please submit your name and email address no later than Wednesday, July 12th by emailing MHPD-stakeholders_intervenants-DPSC@hc-sc.gc.ca