5th Annual

EU Medical Device Regulation Conference

July 12-13, 2023 | Virtual Event

Clarifying the Recent Amendment to the EU MDR Transition Period, all while Pursuing with Ongoing Projects to Achieve Timely Compliance for New & Legacy Devices with a Focus on Mastering Tech File Development to Streamline Notified Body Reviews

Program Overview

This event brings together regulatory, legal, and global regulatory agency perspectives to share strategies and methodologies on current challenges faced by medical device regulatory affairs teams working to secure product approval. Explore how your peers educate and engage internal stakeholders in clinical research/performance evaluation, quality assurance and post-market surveillance to gather and fulfill submission requirements in multiple global markets. Case studies and group discussions highlight practical experiences among shifting regulatory expectations.

The dynamic Q1 Productions virtual platform fosters a sense of collaboration. Thoughtfully designed networking features connect you with your peers beyond the capabilities of a Zoom meeting. Customize your experience and address your unique concerns during live Q&A after each session. Our commitment to industry perspectives keeps the program focused on what matters and dynamic session formats to increase interactivity and strategy-building.

Countdown to the EU Medical Device Regulation Conference:

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Experience the Quality First Difference.

Learn from Industry Leaders

An exclusive experience with professional thought leaders provides you with direct insight into current solutions.

Keep up with Industry Trends

Learn through dynamic panel discussions, case studies and real world evidence on current topics directly related to your industry.

Exchange Ideas & Network

We provide a platform for your team to ask questions with experienced industry experts. The key to building your knowledge and seeing things from another perspective.

Find Solutions that Work for You

Insight and interaction are at the ready for you and your team. Collaborate with your peers, utilizing their insight and experience to accommodate your common challenges.

“I gained information on the path industry is taking. The Q1 staff were all a joy to work with.”

Mitch Mallough, Program Engineer III, Johnson & Johnson

Distinguished Presenters Include:

Gretchen Adams
Technical Director Medical
DEKRA Certification Inc.

Tania Pearson
Regulatory Systems Director
MEDTRONIC

Erik Vollebregt
Partner
AXON LAWYERS

View Full Agenda

Join our LinkedIn Group to stay up-to-date on all things Medical Device Regulatory

The Q1 Productions Virtual Event Experience

Reach out to us with any questions.

Our team will respond promptly!

Chris Cockerell
Senior Event Manager
Q1 Productions
+1 (312) 224-8722
ccockerell@q1productions.com

www.q1productions.com

Purdie Pascoe is a healthcare market research company based in London, UK. Since 2018 they have expanded their services to help medical device manufacturers implement Post Market Clinical Follow-up (PMCF) surveys. They have developed a best-practice approach, approved by EU regulators and compliant with GDPR regulations, for high quality PMCF surveys (both at physician / end user level and at patient level). They support manufacturers from design through to the reporting of PMCF surveys, having already completed more than 300 bespoke PMCF surveys for several of the leading medical device manufacturers, across a variety of device types and risk classifications.

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The Highest Standard

Guiding our clients through the domestic & international regulatory maze since 1999.

Our team of consultants has expertise in the most current and ever-evolving global regulations and certifications to provide comprehensive premarket and post-market support. We assist our clients in finding the most effective means to mitigate risk and achieve their goals using proven methodologies and industry best practices.

Because regulatory authorities hold you to the highest standard, you can hold us to the same. With you every step of the way, we’re committed to launching safe, compliant products into the global market as efficiently as possible.

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At Veranex, we can help you with concept through to commercialization by enabling:
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At every stage, we navigate our clients to realize efficiencies in cost and time with our integrated and comprehensive solutions.

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Since TrainingPros was founded in 1997, we have been dedicated to helping our clients find the right consultant for their projects. 25 years later, we are proud to have helped hundreds of clients complete their projects and thousands of consultants find great assignments. We continue to focus on helping our clients and consultants as well as our community as a certified women-owned, award-winning staffing company that works exclusively with Learning & Development professionals to match consultants to client projects.

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TELCOR is the proven leader of health care software solutions for revenue cycle management (RCM) software and services designed specifically for laboratories. TELCOR RCM, our SaaS solution, and TELCOR Revenue Cycle Services, our billing service, are designed to streamline workflow, improve collections, and provide real-time analytics. Our software and service solutions are designed for the unique challenges and requirements of laboratory specialties and the clients they serve. With full access to data, labs have complete visibility of their data and can track key performance indicators. No other vendor works as hard ensuring you get paid for the work you do.

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At Tipping Point Media, we pride ourselves on developing innovative, creative, and technically advanced virtual training and digital marketing solutions for the life sciences industry.

We push the limits of what's possible using Augmented and Virtual Reality to create revolutionary experiences proven to increase audience engagement and retention rates.

Our dedicated team of educators, medical experts, certified programmers, and digital renaissance innovators are committed to creating high-quality custom creations that bring your company's vision to life.

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VantagePoint Performance trains Salespeople to be more fluent and comfortable across different situations needing different sales approaches, and we train Sales Managers to be better coaches and team leaders, with more focus and less stress.

We’re different from the average sales training company because:

We don’t believe that one approach, one system, or one methodology is absolutely superior. All have something to offer, and the “best approach” or “best system” depends on the sales situation. This is what our applied, academic research tells us.
Our use of data science, specifically Machine Learning, helps us learn about our clients more meaningfully. We provide insights from each client’s data to help them understand what drives the success of their top-performing Salespeople and Sales Managers.
We are constantly feeding what we learn back into our training products, and we invest a bigger slice of our total energy into this innovation than the average sales training company. Our clients can access always-refreshed intellectual property and content through our training subscriptions.

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Policy Reporter, acquired by TrialCard in 2019, provides innovative healthcare software solutions to track payer policies in near real-time and enhances market access for the therapies patients need most. The company’s patented software-driven solutions include a suite of billing and reimbursement tools for providers and laboratories, market intelligence tools for payers, and a suite of market access solutions for life science companies. Its clients include some of the world’s largest pharmaceutical and healthcare companies.

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5th Annual

EU Medical Device Regulation Conference

July 12-13, 2023 | Virtual Event

Clarifying the Recent Amendment to the EU MDR Transition Period, all while Pursuing with Ongoing Projects to Achieve Timely Compliance for New & Legacy Devices with a Focus on Mastering Tech File Development to Streamline Notified Body Reviews

Program Overview

Countdown to the EU Medical Device Regulation Conference:

Experience the Quality First Difference.

Learn from Industry Leaders

Keep up with Industry Trends

Exchange Ideas & Network

Find Solutions that Work for You

“I gained information on the path industry is taking. The Q1 staff were all a joy to work with.”

Mitch Mallough, Program Engineer III, Johnson & Johnson

Distinguished Presenters Include:

Gretchen Adams Technical Director Medical DEKRA Certification Inc.

Tania Pearson Regulatory Systems Director MEDTRONIC

Erik Vollebregt Partner AXON LAWYERS

Join our LinkedIn Group to stay up-to-date on all things Medical Device Regulatory

The Q1 Productions Virtual Event Experience

Reach out to us with any questions.

Our team will respond promptly!

Chris Cockerell Senior Event Manager Q1 Productions +1 (312) 224-8722 ccockerell@q1productions.com

Gretchen Adams
Technical Director Medical
DEKRA Certification Inc.

Tania Pearson
Regulatory Systems Director
MEDTRONIC

Erik Vollebregt
Partner
AXON LAWYERS

Chris Cockerell
Senior Event Manager
Q1 Productions
+1 (312) 224-8722
ccockerell@q1productions.com