Part of your month, every month: R&Q Intelligence Series webinars are held on the fourth Tuesday of every month. These free webinars from some of the medical device industry's leading-most experts are designed for reporting on and analyzing the top industry trends and topics in the medical device space, each providing key and actionable takeaways for attendees. Slides and recordings will be made available to all registrants. Next up: April 25th, where we'll discuss EU MDR.

Medical Device FDA Audit and Health Canada Audit Webinar

What? 

Please join us for a free R&Q Intelligence Series webinar:
MDSAP: What is it? Is it for me? How will I get it done in time?

The session will be held on Tuesday, March 28th from 1:00pm - 2:00pm EST. The learning opportunity is free.

 

MDSAP can potentially offer a variety of important advantages.

While currently optional for FDA, it will be mandatory for Health Canada in January of 2019. Times will be busy with limited qualified registrars, ISO 13485:2016 implementation by March 2019, and EU MDR by 2020.

Attend this webinar if you want to understand MDSAP inside and out and be sufficiently prepared.

Having been on the receiving end of two MDSAP audits, special R&Q Intelligence Series guest Connie Hoy of Cynosure Inc. (recently acquired by Hologic) will describe her successful first-hand experiences and offer step-by-step practical advice on how to adequately prepare for MDSAP and be successful. Her recent real-world case studies provide the perfect examples of what to do and how to accomplish it.

During the session we will cover:

  • Brief background, description, and why the program was put into place
  • Who is impacted and when? (including what happens in the EU)
  • How is the program used by regulatory authorities?
  • What are the MDSAP audit and result review processes?
  • Pros and cons of participation
  • How to participate?
  • Auditing organization (BSI, TUV, Intertek) bottlenecking
  • Case studies featuring practical implementation
  • What to do: R&Q recommended next steps

When we're done, you'll leave with:

  • An excellent understanding of the MDSAP program
  • Knowing how it might impact your company
  • A clear understanding of your potential next steps
  • Practical tips and guidance for actual implementation

 

 

We are passionate about your success. Tell us more about your regulatory and quality needs so we can help.

Book a Consultation

GLOBAL BOTTOM CTA INSTRUCTIONS:

To display custom copy instead of global copy in this section, please go to Show Global Content for Bottom CTA? toggle in the "Contents" tab to the left, toggle it off, save, and then REFRESH the page editor, the custom text will then show up and ready to be edited.

Turning the global content back on will be the same process, go to the toggle and toggle it back on, save and refresh!