Worried about the FDA knocking on your door? Wish you could protect your company from unwarranted inspections?
Did you know the FDA has endorsed:
• ISO 13485:2016 as the basis of the QMSR?
• MDSAP certification?
Did you also know MDSAP certification will help protect medical device manufacturers from unannounced and unwarranted FDA inspections?
This free, one hour webinar addresses why manufacturers should get their internal audit program MDSAP compliant and their auditors MDSAP trained.
You will learn:
• The power of having a trained MDSAP auditor
• Guidance on how to prepare your QMS to be compliant
• The many benefits of achieving MDSAP certification
Markus Gee is the Director of Axeon’s Medical Device Division. Markus has over 30 years of hands-on Quality System Management, auditing, training facilitation and consultation experience. He’s been “boots-on-the-ground” in R&D, Product Development, Manufacturing, Regulatory, Quality, Supplier Relations, etc. He invites you to watch this free webinar to refresh and build your quality skills.
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