“…Of all the suppliers I have used over the years ComplianceAcuity earned my highest recommendation…”
GMP Training Attendee
“…Kevin committed himself to understanding our business model, products and processes before tailoring training and compliance solutions for our firm. This has been greatly beneficial to our firm from an economic and time perspective as it has built on our systems and processes rather than starting again…”
COO – Class II device Manufacturer
“…Providing not only the answer, but the reasoning used by regulatory agencies was instrumental not only to our device approval, but to managing the product as a whole…”
President, Chief Engineer – Software Device
“…Thanks! This [EU MDR Clinical Evaluation Plan] looks very good…”
Regulatory Compliance Manager
“…The EU MDR SOPs were great and much appreciated. With all the labeling work that I had to do, it would have been very easy for me to just overlook the SOPs or to make them so generic that they wouldn’t be useful….”
Chief Operating Officer
“…We really appreciate your work. Looking forward to an EU MDR invoice. As always, thank you for everything…”
President
“…I was very impressed with the EU MDR Clinical Evaluation Report, by the way. Great job…”
President
“…Wow, your [EU MDR Technical Documentation] work is yet epic again. Much appreciated and that completes my file…Thanks and whew!”
President
“…This [EU MDR Gap assessment] is an amazing work…”
President
“…Good news, I passed the [EU MDR] “Audit” for my technical files…thanks for your work on this…”