Medical Devices Summit Europe


November 11-12, 2013
Dublin, Ireland

November 11-12, 2013

Dublin, Ireland

Untitled Document

Conference Details:

Given the recast of the European Medical Device Directive and the recent changes to the FDA's 510(k), the regulatory climate in the medical device industry is more volatile than ever. Medical Device manufacturers are concerned with staying up-to-date with these regulations, accelerating time to market, reducing cost and improving profit margins. Moreover, expanding into different markets within and outside Europe poses new issues – can you risk not being on top of the latest changes? Opal Events' Medical Devices Summit Europe will address these topics and help you prepare strategies to meet current and to anticipate incoming challenges.

Join us for two days of panels, presentations and networking opportunities with high-level individuals from across the industry as we discuss the hottest issues, including:

Regulatory updates and changes to the 510(k) and the EU Directive
Strategies for successful submissions, maintaining compliance and improving quality
Spotlight presentations on foreign markets, including:
- Expanding into foreign markets
- Integrating best practices into your clinical trials
- How reimbursement varies in different markets
- Usability and device design
- Best practices for international recalls

If you are interested in sponsorship, exhibiting, or speaking opportunities, please contact rsotomayor@opalevents.org

Target Audience:

Opal Events' Medical Devices Summit Europe has been researched and designed specifically for executives from medical device manufacturers, specifically:

Chief Executive Officers
Chief Financial Officers
Chief Operations Officers

Vice Presidents, Directors, Managers, and Engineers of:

Compliance
Quality
Regulatory Affairs
Software Engineering
Outsourcing
Supplier Management
Research & Development
Product Development
Commercial Operations

Testimonials From Last Year's Event:

It is compact, concise and yet very informative and value add summit. Very well prepared and experienced speakers.
-- Varisai Mohammed, Director of Total Quality, INQPHARM EUROPE LTD

Very nice summit. A good networking was possible during the breaks. The list of attendees was impressive.
-- Samantha Glasgow, Quality Assurance & Technical Documentation Officer, Erfa Pharm

One of the best conferences I have attended on Medical Devices. Very educational and enjoyable.
-- Philip Reavey, Senior Technical Manager, Beckman Coulter Ireland Inc.

'The relevant, coherent range of presentations combined with an eclectic mix of personalities was perfect. An essential diary entry for 2013,'
--Jonny Dobbin, Quality Analyst, Armstrong Medical Ltd.

Very enjoyable two days. Good mix of serious discussions and entertainment between sessions. Met lots of interesting people. Highly recommended.
-- Liam Mulloy, Managing Director, Vascular Solutions Zerusa Limited

An engaging, well hosted conference with a good balance of subjects, well covered by knowledgeable speakers.
-- Ian Quirk, Worldwide Director of Clinical & Regulatory Affairs, Ranier Technology

Hotel Info:

TBA

Conference Registration Prices:

Early Bird Rate

Standard Rate

Service providers & vendors (including contract manufacturers, consultants and legal groups)

$795

$995

Employees of Medical Device Manufacturers (OEMs), Non-Profit organizations, Government and Academic faculty*

First 100 free*, after $495

Registration price reflects $100 online discount

*Institutional End-Investors include: organizations that are solely investing on their own behalf in alternatives and do not sell any alternative investment products or services to clients including; sovereign wealth funds, pension funds, endowments, foundations, family offices, private clients and treasury.

Sponsorship, Exhibition & Speaking Opportunities
Call: 212-532-9898 x 0
Email: information@opalevents.org

Diamond Sponsor:

Gold Sponsor:

Silver Sponsor:

Media Partner:

Untitled Document

2012 Attendees & Agenda

Global Product TPM QA Manager, Abbott
Global Product TPM QA Manager, Abbott
Internal Auditor, Abbott
Internal Auditor, Abbott
Manufacturing Engineer, Abbott
Manager Regulatory Affairs, Abbott
Regulatory Affairs Specialist, Abbott
Director, Regulatory Compliance, Quality Systems and Government Affairs, Abbott
Senior Technical Specialist, Abbott Diagnostics
Regulatory Affairs Associate, Abbott Vascular
Director International Regulatory Affairs, Abbott Medical Optics
Associate Director, Devices, Regulatory Affairs, Abbott Nutrition International
Director of Engineering, Acuitas Medical
Regulatory Affairs Manager, Advanced Medical Solutions
QA/RA Manager, Advanced Surgical Concepts
Development Engineer, Advanced Surgical Concepts
President, Aegis Medical Innovations
Quality & Regulatory Affairs Manager, Agfa Healthcare
Quality Assurance Manager, Allergan Pharmaceuticals
Strategic Planning and Business Development Manager, Alvimedica
Senior Consultant, Alvimedica
Executive Director, Raw Material Device Supply Chain, Amgen
Regulatory Affairs Coordinator, Amway GmbH, Germany
Marketing Manager, Aptiv Solutions
Quality Assurance Specialist, Argutus Medical
General Manager, Argutus Medical
Clinical Services Director, ArjoHuntleigh
Quality Manager, Armstrong Medical
Technical Assistant, Armstrong Medical
Technical Assistant, Armstrong Medical
Certification Engineer, Product Configuration＆Conformity, Ascom AB
Certification Engineer, Product Configuration＆Conformity, Ascom AB
Marketing Manager, Aspect Imaging
President, Association of Medical Device Reprocessors
Senior RA Specialist, Bard
Director of Business Development, Bard
System Support Manager, Beckman Coulter Ireland
Senior Technical Manager, Beckman Coulter Ireland
Regulatory Affairs Specialist, Beckman Coulter Ireland
Regulatory Affairs Specialist, Beckman Coulter Ireland
Contract Manufacturing/QA/RA, Becton Dickinson
Director of International Regulatory Affairs, Bess AG
Managing Director, Bestic AB
Clinical Advisor, BioBusiness
Quality and Regulatory advisor, BioBusiness
CEO, BioBusiness
Project Manager, BioBusiness
Legal Counsel, Biocartis
General Counsel, Biocartis
Associate Director, Devices, Global Regulatory Affairs, Biogen Idec
Fellow, BioInnovate Ireland
Fellow, BioInnovate Ireland
Fellow, BioInnovate Ireland
Research Fellow, BioInnovate Ireland
Research Fellow, BioInnovate Ireland
Research Fellow, BioInnovate Ireland
Research Fellow, BioInnovate Ireland
R&D Engineer, Boston Scientific
QA Manager, Boston Scientific
Regulatory Compliance Specialist II, Boston Scientific
Senior Quality Engineer, Boston Scientific
Senior Product Development Manager, Boston Scientific
QA/RA Manager, Cappella Medical Devices Limited
VP Business Development, Cappella Medical Devices Limited
Vice President of Regulatory and Clinical Affairs, Cappella Medical Devices Limited
Business Development Manager, Cardicell
Business Development Manager, Cardicell
PhD Researcher, Cardiff University
Director, Marketing and IR, Carmat SA
Coordinator, Central Remedial Clinic
Senior Manager, Central Remedial Clinic
Consultant, Central Remedial Clinic
Manager, Central Remedial Clinic
Board Observer , CeQur
CEO, Cognition Corporation
Sales Engineer, Cognition Corporation
Senior Application Engineer, Cognition Corporation
Director, Cognition Corporation
Director, Cognition Corporation
VP, Costumer Success, Cognition Corporation
QA Director, Contura International
QA/RA Lead, Cordis Cashel
Quality Manager, Covidien
Quality Systems Engineer, Covidien
Senior Research Fellow, CRANN Institute
Marketing and Operations Director, Deltex Medical
Industrial Engineer, Design Partners
Medical Design Director, Design Partners
Dental Materials, Dublin Dental University Hospital
Biomedical Lecturer, School of Mechanical & Manufacturing Engineering, Dublin City University
Senior Researcher, Dundalk Institute of Technology
SFI Stokes Lecturer and Principal Investigator, Dundalk Institute of Technology
CFO, Eegapps Medical Limited
Director and Company Secretary, Eegapps Medical Limited
Director of Quality Assurance & Regulatory Affairs, Europe & AFLAME, Elekta Limited
Senior Systems Engineer, Elekta Limited
Corporate Account Manager, Elsevier
Customer Engagement Manager, Elsevier
Product Development Manager, Embase
Quality Assurance and Technical Documentation Officer, Erfa Pharma
Deputy Head of Unit, Medical Devices, European Commission
Partner, Finnegan, Henderson, Farabow, Garrett & Dunner
Attorney, Finnegan, Henderson, Farabow, Garrett & Dunner
Entrepreneur in residence, Florida Institute for the Commercialization of Public Research
Researcher, Fondazione Filarete
PhD, Fondazione Filarete
QA/RA Manager, Fortimedix BV
QS Complaint Manager, Fresenius Medical Care
Co-Founder and Chairman, G9MD
Lecturer, Galway-Mayo Institute of Technology
Project Manager, Genzyme
Marketing Director, German Healthcare Industries
CEO, GlySure
Vice President Business Development, GripTip
Clinical Research Manager, HeartSine Technologies
GLP/GCP Specialist, HeartSine Technologies
Quality Assurance Specialist, Hologic
CEO, Hygieia
VP Sales and Marketing, Hygieia
VP Products, Hygieia
Chairman, Incereb
CTO, Incereb
Director of Total Quality, Inqpharm Europe
Lecturer, Institute of Technology, Sligo
Director , Institute of Testing and Certification
EMEA Medical Devices, Intel
Regulatory Affairs Officer, Intelesens
Scientific Officer, Irish Medicines Board
Scientific Officer, Irish Medicines Board
Director, Isomed Limited
Regulatory Controller, Isomed Limited
Representative, Isomed Limited
Representative, Isomed Limited
Partner, Patent Attorney, J A Kemp

Masters in Public Health Student, Johns Hopkins Bloomberg School of Public Health
Managing Director, Kingdom Healthcare Limited
Clinical Research Physician, Kuros Biosurgery AG
Product Manager, Lacer
Medical Doctor, Lafia Hospital
Partner, Launch Global
Chief Regulatory Officer, Leman Micro Devices
Research Fellow, London School of Economics
Global Regulatory Officer, Lutronic
Sales and Marketing Director, M3AT
Business Manager, Meditech Strategic Consultants B.V.
Regulatory Affairs Specialist, Medix Biochemica
Regulatory Compliance Manager, Metabolomic Diagnostics
Sr. Director Corporate Strategy Development, Mindray
CEO, Mitamed
Business Development Director, Moravia
CEO, Nasseo
Product Development, NGE Technologies
Director of Regulatory and Quality, Novate Medical
Clinical Design and Assurance, Novate Medical
Partner of Medical Devices, NSF-DBA
Research Fellow, NUI Maynooth
Research Fellow, NUI Maynooth
Research Associate, NUIG
Engineer, NUIG
PhD Researcher, College of Engineering and Informatics, NUIG
Quality, Regulatory and Clinical Affairs Director, Nuubo
RA/QA Manager, Oceana Therapeutics
General Manager – Managed Service, Olympus KeyMed
Quality Manager, Olympus KeyMed
COO, OncoMark
Postdoctoral researcher, OncoMark
Managing Director, Orbimed Advisors
Quality and Regulatory Affairs Manager, OrganOx Limited
Medical Science Liaison, Orthofix SRL
Developer, OS – Elektronik
Director, OsteoMed
Chief Engineer, Otodynamics
Production and Development Support Engineer, Otodynamics
Clinical Lecturer, Our Lady’s Hospice
Board Member, Paul Hartmann
Sales Management, Paul Hartmann
Medical Director, Oncology, Pfizer Global Research
Clinical Research Manager, Phagenesis
International Business Development Director, Pharmafilter
Software Team Leader, Philips
Quality Manager, Philips
CEO, Profector Life Sciences
Doctor, Profector Life Sciences
Doctor, Profector Life Sciences
Doctor, Profector Life Sciences
Doctor, Profector Life Sciences
Verification & Validation Manager, Quanta Fluid Solutions
Msci, Quanta Fluid Solutions
CEO, Ranier Technology
Regulatory Affairs Manager, Ranier Technology
Worldwide Director of Clinical & Regulatory Affairs, Ranier Technology
Business Development, Raumedic AG
Manager, Real Staffing Group
Head of Design Verification, Roche Diagnostics
Post Doctoral Researcher, School of Pharmacy, Royal College of Surgeons in Ireland
Senior Lecturer in Pharmaceutics & Program Director, School of Pharmacy, Royal College of Surgeons in Ireland
Regulatory, Compliance, & Quality Technician, Salts Healthcare
Quality Manager, Salts Healthcare
Quality & Regulatory Technician Support, Salts Healthcare
North American Sales Manager, Seapine Software
VP of Worldwide Sales, Seapine Software
CEO, Sedana Medical AB
COO, Sedana Medical AB
Purchasing and Marketing Manager, Sedana Medical AB
RA Specialist, Sorin Biomedica Cardio
Vice President, Spectral MD
CEO, SpineForm
Programme Manager, Centre for Advanced Medical Imaging, St. James’s Hospital
Research Fellow, St. James’s Hospital
Specialist II, Regulatory Affairs, St. Jude Medical
RA Team Leader, Stryker
Quality Engineer, Stryker
Regulatory Specialist, Stryker
CEO, Surgacoll Technologies
Quality Manager, Surgacoll Technologies
Partner, T4Analytics
Director of RA, EMEA, Teleflex Medical
RA Specialist, Teleflex Medical
RA Specialist, Teleflex Medical
CEO, Tensive
CEO, TMG-BMC
Head of R&D, TMG-BMC
Assistant Professor, Physiology Department, Trinity Biomedical Sciences Institute
Researcher, Trinity Biomedical Sciences Institute
Researcher, Trinity Biomedical Sciences Institute
Researcher, Trinity College Dublin
Researcher, Trinity College Dublin
Researcher, Trinity College Dublin
PhD Researcher, Trinity College Dublin
Medical Professor, Trinity College Dublin
Lecturer, Department of Pharmacology & Therapeutics, Trinity College Dublin
Health Innovation Lead, Centre for Practice and Healthcare Innovation, Trinity College Dublin
Business Development, Tyndall
Senior Scientist, UCC
Commercialisation Specialist, UCC
General Manager, UCC
Business Development Manager, UCD Conway Institute
Managing Director, U-drain
Regulatory Director, United States Blood Bank
Senior Lecturer, University College Cork
Senior Scientist, University College Cork
Commercialisation Specialist, University College Cork
Director, Biomedical Facility, University College Dublin
Biomedical Researcher, University College Dublin
Researcher, University of Limerick Microbiology Laboratory
Head of Department, University of Limerick Microbiology Laboratory
Researcher, University of Limerick Microbiology Laboratory
Student, University of Oxford
Managing Director, Vascular Solutions Zerusa Limited
Quality and Regulatory Consultant, Veryan Medical
Product Specialist, Gore PharmBIO Products, W. L. Gore & Associates GmbH
Senior Regulatory Engineer, Welch Allyn
Regulatory Engineer, Welch Allyn
Director, Xeolas Pharmaceuticals
Director, Xeolas Pharmaceuticals
RAQA, Xeridiem
Vice President QA/RA EMEA, Zimmer
Regulatory Affairs Specialist, Zimmer
Associate Director, Quality Assurance, Zimmer
Quality and Regulatory Compliance Independent Consultant
Software Solutions Consultant

2012 Agenda (current as of 11/09/12)

Past Conference Day 1: Tuesday, 13 November 2012

9:15

Continental Breakfast & Registration

10:00

Opening Remarks

10:05

Chair's Welcome and Audience Demographics:
Learn who is in the room so that you can identify your peers and people with whom you would like to network.

David Cronin, CEO, COGNITION CORPORATION

10:15

THE PROPOSAL FOR REVISION OF THE EUROPEAN MEDICAL DIRECTIVE

Erik Hansson, Deputy Head, Health Technology & Cosmetics, EUROPEAN COMMISSION, DG HEALTH AND CONSUMERS

11:00

Morning Refreshment & Networking Break in the Exhibitors' Hall

Talk with your peers, enjoy some light refreshments - all while learning about new and exciting services and technologies from our exhibitors.

11:30

ADAPTING TO REVISION THE RECAST OF THE EUROPEAN MEDICAL DEVICE DIRECTIVE

Analyse the industry response to the Council that harmonises the laws relating to medical devices within the European Union.
Assess how the modifications to the directive affect your product.
Discuss the “immediate measures” brought by the Directive
Prepare for the additional review for high risk devices in the EU

Ian Quirk, Worldwide Director of Clinical & Regulatory Affairs, RANIER TECHNOLOGY LIMITED

12:15

UNPACKING THE AMERICA INVENTS ACT: IMPLICATIONS FOR THE MEDICAL DEVICE INDUSTRY

Preparing your patent portfolio for the U.S. patent law changes, including the change to a "First-Inventor-to-File" System.
Understanding new mechanisms to challenge IP roadblocks and the business and strategy considerations in their use
Using the European Patent Convention and the America Invents Act together to build strategic advantages over competitors

Eric Raciti, Partner, FINNEGAN, HENDERSON, FARABOW, GARRETT & DUNNER, LLP
Jeremy P. Bond, Attorney, Finnegan, Henderson, Farabow, Garrett & Dunner, LLP

12:45

SPOTLIGHT ON NOTIFIED BODIES: SELECTING THE RIGHT PARTNER

Establish best practices for choosing your notified body; what specialties matter.
Determine whether the notified body you work is up-to-date with foreign regulatory practices.
Learn key strategies for developing a comprehensive post-market surveillance program.

Matthias Buerger, Vice President, Quality Assurance & Regulatory Affairs – EMEA, ZIMMER GMBH
Stefan Menzl, Director International Regulatory Affairs, ABBOTT MEDICAL OPTICS INC.

13:35

SECRETS TO UNLOCKING THE VALUE IN YOUR COMPANY TO ATTRACT U.S. VENTURE CAPITAL INVESTMENT

Learn how to affordably assess the U.S. Market for medical devise expansion
Understanding best in class “bridge services” for soft landing in U.S. for high-growth start-ups and later stage companies
Review reasons behind successful & failed funding strategies from North America,, Europe & Asia
The Bestic experience-from Sweden to the US

Paul F. Lavallee, Partner, LAUNCH GLOBAL
Catharina Borgenstierna, CEO, BESTIC AB

14:00

LOOKING OUTSIDE THE BOX: NON-CONVENTIONAL FINANCING SOURCES

There are more options out there than the standard VC model
Learn about other types of capital available
Identify situations for alternative financing structures

Matthew Rizzo, Managing Director, ORBIMED ADVISORS LLC

14:20

Networking Luncheon

15:20

EXPLORING EMERGING MARKETS

Expand into Turkey, India, Iran, Brazil, and Mexico.
Examine the potential for device development in Eastern Europe.
Identify who the stakeholders are in new markets.
Determine the validity of contracts in developing markets and your ability to enforce them.
Build a regulatory strategy to adapt to different regulations.
Understand which markets require ISO certification.

Can Küçük, Strategic Planning and Business Development Manager, ALVIMEDICA

15:45

SCALABLE THERAPEUTICS MEDICAL PLATFORM
In this marquee collaboration between Intel and Wind River, hardware and software come together to show the potential of Intel architecture in critical care therapeutics devices – in this case an infusion pump application. The proof of concept highlights how a full Intel solution can help support the development of a more connected, secure, and scalable medical device.

Conor A. Clancy, Market Development Manager, Intelligent Systems Group, EMEA, INTEL CORPORATION

16:20

Afternoon Refreshment & Networking Break in the Exhibitors' Hall

16:45

MANAGING A NICE MTAC SUBMITTAL

Graham Lowe, Marketing and Operations Director, DELTEX MEDICAL

17:15

Day One Closing Remarks and Cocktail Reception (in the Exhibitors' Hall)

Sponsored by:

Past Conference Day Two: Wednesday, 14 November 2012

8:15

Continental Breakfast & Registration

8:50

Opening remarks from Opal- wrap up from Day 1 and looking ahead

9:00

HANDLING POST-MARKET PROMOTION, INSPECTIONS, AND COMPLAINTS

How to prepare for a PMS notified body audit
Strategise how to address complaint systems abroad.
Learn strategies for keeping compliance.
Determine issues in international advertising.

Philippe Auclair, Director, Regulatory Compliance, Quality Systems & Government Affairs, ABBOTT VASCULAR INTERNATIONAL BVBA

9:30

ROUNDTABLE WORKSHOPS

Choose (2) half hour long workshops to attend, and join other industry leaders as they host in-depth discussions on a variety of topics.
After 30 minutes, attendees will be given the opportunity to switch rooms and hear from a different industry leader on different topic.
Remember to sign up for your workshop early to ensure your seat!

WORKSHOP 1

Cockpit - Using Modern Tools to Win: Working with Medtronic
Customer needs... user experience... stakeholder requirements... system features... safety... validation... and complete traceability, how in the world do you get it all done? Even harder, how do you get it all done efficiently and with the least pain? Whether you're a start-up or one of the big guys, modern tools are simplifying your burden. In this workshop, you will see what one of these tools looks like, and if you deal with the topics above and this example doesn't feel like it would simplify your life, then we'll buy you a beer.

Mitch Hayes, Vice President of Customer Success, COGNITION CORPORATION
David Cronin, CEO, COGNITION CORPORATION

WORKSHOP 2
AN IN-DEPTH LOOK ON HOW TO UNLOCK VALUE IN YOUR COMPANY AND ATTRACT FINANCING – PART II

Paul F. Lavallee, Partner, LAUNCH GLOBAL
Catharina Borgenstierna, CEO, BESTIC AB

WORKSHOP 3
MEDICAL DEVICE SECURITY: CASE STUDIES & DEMOS

Bart Pestarino, CISSP, Marketing Security Specialist, CODENOMICON LTD

10:30

Morning Refreshment & Networking Break in the Exhibitors' Hall

Talk with your peers, enjoy some light refreshments - all while learning about new and exciting services and technologies from our exhibitors.

11:00

CONDUCTING MEDICAL DEVICE SAFETY AND PERFORMANCE ASSESSMENTS USING EMBASE

Anne Marie Roche, Customer Engagement Manager, Science & Technology Division, ELSEVIER

11:45

SECURITY VERIFICATION AND VALIDATION (VnV) FOR MEDICAL DEVICES

Pragmatic approach for security VnV during the device development lifecycle
Simulation best-practices and MDISS Unknown Vulnerability Framework 1.0
Standardizing security VnV for medical device manufacturers and healthcare delivery organization buyers

Bart Pestarino, CISSP, Marketing Security Specialist, CODENOMICON LTD

12:30

IMPLEMENTING A REQUIREMENTS MANAGEMENT SYSTEM – OUR JOURNEY

Understanding our needs for a Requirements Management System
The key selection criteria for choosing a system
Defining an intuitive controllable process
Implementing a usable process in Cognition Cockpit via workflows and documents
Working together to solve problems

Mark Wallace, PhD, Verification and Validation Manager, QUANTA FLUID SOLUTIONS
Ben Higgitt, MSci, Lead Verification Engineer, QUANTA FLUID SOLUTIONS

13:15

Networking Luncheon

14:15

MEDICAL DEVICE INNOVATION – SOFTWARE AND MOBILE APPS

Medical regulatory compliance using agile software development.
Determine if your app can be considered a medical device.
Identify regulations in software for medical device integration.

Wim van de Goor, Software Development Team Leader, PHILIPS INNOVATION SERVICES
Peter McCaffery, SFI Stokes Lecturer and Principal Investigator - Department of Computing & Maths, DUNDALK INSTITUTE OF TECHNOLOGY
Rhona McAteer, Quality and Regulatory Advisor, BIOBUSINESS LTD.
Peter Donnelly, CEO, BIOBUSINESS LTD.

15:00

STRATEGIES AND LESSONS LEARNED IN INTERNATIONAL DISTRIBUTION

Depict best practices in international supplier management.
Discuss the advantages and pitfalls of partnering with a distributor.
Identify distributor alternatives such as opening abroad offices or partnering with other companies.
Understand how the 510(k) and impacts your power over product sales.
Obtain reimbursement coverage in foreign markets.

Chris Jones, CEO, GLYSURE LIMITED

15:45

SMALL EU COMPANY PERSPECTIVE: GAINING A FOOTHOLD IN US AND INTERNATIONAL MARKETS

FDA approval does not automatically translate into sales in 50 states.
What distribution channel suits you best?
Estimate the cost of doing business in the US.
Consider whether there is a ROI before entering new markets beyond the US and EU.
Tax and legal hurdles need to be overcome before entering the market
Ensure you have commercial and technical agreements in place to cover all eventualities

Liam Mulloy, Managing Director, VASCULAR SOLUTIONS ZERUSA LIMITED

16:30

Conference Adjourns

Service providers & vendors (including contract manufacturers, consultants and legal groups)

$995.00

Qty:

Students

$95.00

Qty:

Employees of Medical Device Manufacturers (OEMs), Non-Profit organizations, Government and Academic faculty*

Regular Price: $495.00
Price: $0.00

Qty:

Clients who registered for this event also registered for

Medical Devices Summit Midwest


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