Australia’s Therapeutic Goods Administration (TGA) has introduced the IRIS InSite program which encourages Health Facilities to submit adverse event reports.
Archives for March 2016
Just in case you missed it – the long awaited 2016 update to ISO 13485 was published at the end of February. This revision is a big shake up of the venerable devices quality standard. It’s going to need time, effort and planning for transition to the 2016 edition. Join us in Adelaide for an intensive workshop on how to make the change.