Understanding the Medical Device Single Audit Program and How to Prepare for it
This webinar was hosted by Kyle Rose, the President of Rook Quality Systems.
You will find this webinar helpful for preparing the registration process with MDSAP program, which allow medical device manufacturers to have a single quality management system audit that meets the requirements of all participating Regulatory Authorities. The initial participating Regulatory Authorities include FDA (USA), TGA (Australia), MHLW (Japan), Health Canada (Canada), and ANVISA (Brazil).
Please contact us at info@rookqualitysystems.com if you have any questions.
Sponsored by
