I have a friend that needs a consultant with experience in preparing for Medical Device Single Audit Program (MDSAP) specifically for Health Canada and FDA.  They already have a contract/agreement scheduled for a two-phase audit with InterTek Inc. and needs immediate help preparing for it.

·  Medical Device Single Audit Program (MDSAP) specifically for Health Canada and FDA

·  ISO 13485 standard for Class 1 Medical Device, non-implantable proprietary dental prosthesis tools, and parts