Get a professional, local Medical Device auditor that's experienced in your industry, at a price you can afford.
“We are a start-up Medical Device company located in Minneapolis. Quality Auditing was able to provide an experienced, credentialed auditor to perform an Internal Audit on short notice to help us prepare for our MDSAP certification. We would highly recommend Quality Auditing for anyone interested in expert auditors!”
— Blake I., QA Manager
How it works:
“We are a manufacturer out here in Chatsworth, California. We make medical device components for our customers under the ISO 13485:2016 standards. QA’s Lead Auditor was very nice, professional and very thorough and was "on the ball". She spotted the "grey" areas that were previously missed. Kudos to Quality Auditing. I'm looking forward to working with them again next year.”
— M. Truman, QA Director
We make it easy for you.
We understand the importance of industry knowledge—it’s the heart of our business. Our deep experience working across different sectors, standards, and regulations enable us to understand your challenges in the compliance landscape but also provide strategic insights and current market intelligence to help you achieve excellence.
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Simply click the button below, fill out the quick form and we’ll get in touch ASAP to get you a quote.
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You’re a busy professional with lots to do. We’re professional medical device auditors with experience performing thousands of audits.
Let us take auditing off your hands forever—so you can focus on what matters most.
We know ISO 13485 & country-specific regulations in and out.
No Travel Expense
Industry Experts
Local Auditors
We’ve honed our expertise working with organizations that range from globally recognized brands to small, family-owned companies in more than 25 countries. Start-ups and established multinationals choose Quality Auditing as their partner to achieve and maintain compliance with global standards & regulations. This positions us to provide unique insights that you can’t find anywhere else.
Device safety & quality are non-negotiables in the medical devices industry. Regulatory requirements are increasingly stringent throughout every step of a product’s life cycle, including service & delivery. We help organizations in the industry demonstrate their quality management processes and ensure best practice in everything they do.
1. Get a quote
2. Schedule your audit
3. We audit for you
Certified Auditors
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Frequently Asked Questions
How are your auditors trained?
Our Medical Device Auditors all have experience in the industry and maintain credentials for ISO 13485:2016 and country-specific regulations. Resumes and credentials are provided as part of the quotation package.
Do you have local and/or worldwide auditors?
Yes! We have many auditors in most major cities across the US as well as Central & South America, Europe, Middle East, South & East Asia. We have auditors that are well versed & seasoned in each industry that we serve.
How much is it going to cost?
Our flat-rate pricing ensures budgeting is easy and you can be assured there will never be additional or unexpected fees. It’s always fair & transparent.
When can you perform the work?
Typically 6 weeks or less. Audits of a longer nature may require some additional time to schedule.
What does the report look like?
We have fantastic reporting. Let us know if you'd like to see one and we'll show you. We are also happy to customize our report format to meet your needs, or work with something you already have established.
How soon can we start?
Right away. Click here or Give us a call: (612) 208-7845
Or Give us a call: (612) 208-7845
Medical Devices Audit Capibilities:
• ISO 13485:2016
• MDSAP - Medical Device Single Audit Program
• US FDA 21 CFR Part 820
• European MDD / AIMDD / IVDD
• New EU MDR / AIMDR / IVDR
• Health Canada CMDR
• Brazil ANVISA
• Australian TGA
• Japan MHLW Ordinance 169
• ISO 14971 Risk Management
• IEC 60601 Electrical Equipment