Preparing for the MDSAP Audit Process
A Case Study from the Manufacturer’s Perspective

Wednesday, July 11, 2018 · 1:30 p.m. - 3:00 p.m. EDT

Devicemakers that export into Canada, Japan, Australia and Brazil face important changes to the audit and inspection process as the new Medical Device Single Audit Program (MSDAP) goes into effect.

The deadline is looming: Canada imposes the new requirements next Jan. 1.

The changes differ in important ways from what you’re used to. Now is the time to get a drop on them.

Mark your calendar for Wednesday, July 11, when consultant Connie Hoy takes you through the changes — what’s the same, what’s different, how you’ll have to alter your thinking.

In 90 lightning minutes, she’ll touch on such key factors as:

  • Using the Companion Document to most successfully prepare for the MDSAP audit
  • Quality system: Insuring that yours completely covers specific country requirements
  • Registration review details: Specifics to expect in this portion of the audit
  • Differences in emphasis: Unfamiliar questions the MDSAP auditor is likely to ask
  • Audit procedures: How the MDSAP audit is conducted and how it differs from FDA inspections and ISO audits
  • “Grading system for nonconforming”: What it really means
  • And much more!

MSDAP audits will be a reality before you know it — less than 6 months. Don’t get caught short. Start figuring things out now with this webinar.

Register now.

BONUS: Order the webinar plus audio recording/transcript or the 24/7 encore plus audio recording/transcript for $487, and receive a FREE copy of CDRH in Transition: Navigating the New Culture of Quality (retail value $397).

CDRH in Transition: Navigating the New Culture of Quality
Don’t let the CDRH’s paradigm shift rock your world! Under the new inspection system, your team of investigators will include at least one specialist in your product area, making it harder to hide your faults. This report outlines the Culture of Quality program’s goals and explains how they will change the way devicemakers will experience inspections.


Who Will Benefit

Devicemakers that export to Canada, Japan, Australia and Brazil will benefit from this presentation in general, as will exporters of high-risk devices; and exporters of combination products to Australia will benefit specifically. Job titles include but are not limited to:

  • Regulatory/compliance
  • Quality assurance
  • Manufacturing/GMP/cGMP
  • Supply chain executives
  • Auditors
  • Legal counsel

Webinar plus Audio Recording/Transcript with BONUS
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$487

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Webinar only
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$287

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24/7 Encore plus Audio Recording/Transcript with BONUS
Learn more

$487

add to cart

24/7 Encore Presentation
Learn more

$287

add to cart

Audio Recording/Transcript
Learn more

$287

add to cart

 

 

 

Meet Your Presenter

Connie Hoy

Consultant
Hoy & Associates Regulatory Consulting

Connie Hoy of Hoy & Associates Regulatory Consulting is a former EVP of Regulatory, Quality and Clinical Development at Cynosure, a division of Hologic, with three decades of experience in the medical device industry.

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA.

Phone (703) 538-7600 | Fax (703) 538-7676 | Toll free (888) 838-5578 | Email customerservice@fdanews.com

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