Whether you’re just starting to plan your IVDR program (or not sleeping well because you haven’t started yet) or well into EU MDR but ready to plan post-market surveillance activities, our September webinar will be helpful.

All registrants will receive access to the slides and recording.

RQ_WB_Program_Management_On_Demand_Promo-min New Branding


Get right to it → This webinar will cover tips, tricks, and lessons learned for successful program/project management of your transition to IVDR or EU MDR certification.

A little more detail...

We all still have our day jobs, right? New product development, sustaining design changes and issues, day-to-day regulatory support… we’re all busy! And now we have to get IVDR certified? How can we do it all? The solution is effective program management.

If you're just starting to plan your IVDR program or well into EU MDR but ready to plan PMS activities, this webinar will be incredibly helpful.

We’ll discuss keys to success and stories from our projects at every phase, including that critical initiation phase that teams often skip over. Resource and communication plans, detailed schedules by product family, metrics, and dashboards are musts for large programs with limited resources.

Join us and pick up some tips on how increase the odds of success for your program.


Sign Up Now ➞



Aurora Hill, MS, MBA, PMP – Senior Project Manager
Regulatory & Quality Solutions (R&Q)

aurora_square-minAurora Hill, a certified project management professional, has 14 years of experience developing, commercializing and sustaining medical device technologies. She has supported several business functions such as corporate development, research and development, operations and business development to lead teams that deliver solutions that meet technical requirements, regulatory requirements and corporate strategic initiatives. Aurora has a master’s degree in biomedical engineering and a master’s in business administration.



Ruthanne Vendy – Senior Principal Specialist
Regulatory & Quality Solutions (R&Q)

ruthanne_vendy_squareRuthanne has been a medical device regulatory professional for more than seventeen years, with experience in multiple medical specialties. Ruthanne started her medical device career in product development with one of the world’s largest manufacturers of professional dental products. She migrated into regulatory affairs early in her career as an RA Associate, and quickly found her niche as an RA Specialist. She spent her last six years prior to joining R&Q as an RA Manager responsible for a diverse portfolio of surgical and dental devices. Ruthanne has worked for several companies in both corporate and manufacturing settings providing staff training, audit management (internal, notified body, and FDA), premarket and post-market support, global registrations and licensing, submissions, document control oversight, labeling/advertising approvals, and technical documentation. Ruthanne also served on the Material Review Board for her last company. She is Regulatory Affairs Certified (RAC) by RAPS, has a Bachelor’s degree in Organizational Management from Eastern University, and holds a Health Services Management Certification from Philadelphia University.


Sign Up Now ➞

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

Book a Consultation


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!