OVER THE PAST TWO DECADES, THE INNOVATION IN THE MEDICAL DEVICES BROUGHT LIFE-CHANGING DISRUPTION BY HARNESSING TECHNOLOGICAL ADVANCEMENTS, WHILE AT THE SAME TIME LOWERING COSTS OF HEALTHCARE. CONSEQUENTLY, MORE AND MORE OF MEDICAL DEVICES FIND PLACE IN THE CLINICS, AMBULATORY CENTRES, OPERATING ROOMS AND IN OUR BODIES…..MORE TO COME HERE!

Dr. EMIR OSMANAGIC
CHAIRMAN OF THE SUMMIT
SENIOR DIRECTOR OF ENABLING TECHNOLOGIES

JOHNSON&JOHNSON / DEPUY SYNTHES

KEYNOTE PRESENTATION

ON: CO-CREATION OF SUCCESSFUL HEALTH TECHNOLOGIES IN THE CONTEXT OF AN INCREASING DEMAND, LESS RESOURCES AND STRICTER REGULATIONS

Dr. NICK GULDEMOND 

Dr. Guldemond is professor Integrated care and technology at Sechenov First Moscow State Medical University and Erasmus University Rotterdam. He holds a degree in medicine and electric engineering. During his career, he worked as a clinical researcher on various clinical and biotechnological research projects and was involved in international programs regarding clinical innovation and medical technology. He is a key expert on eHealth and integrated care for various governments on different continents, international NGO’s, multi-nationals as well as digital start-ups.

KEYNOTE PRESENTATION

ON: CHALLENGES TO INNOVATE IN THE MEDICAL DEVICE INDUSTRY UNDER THE LIGHT OF THE NEW EU MDR – A NOTIFIED BODY PERSPECTIVE

DR. MAX SINGH

Dr. Max Singh is the Global Director of the Orthopedic Focus Team at TÜV SÜD Product Service. Prior to this role, he spent about 15 years in the medical device industry, mainly working in the orthopedic sector. He held several positions in R&D, where he was in charge for designing medical devices for knee, hip, trauma, and spine surgery. He also has strong experiences in computer-assisted surgery (CAS) and surgical robotics. Besides R&D, he was also responsible for product management and marketing of large amounts of product portfolios. Through global launch activities, he was exposed to the international regulatory requirements in the medical device industry.
Dr. Singh holds academic degrees in medical engineering and business administration. In his doctoral research, he investigated various aspects of spine surgery technologies in the U.S. medical device industry. Within TÜV SÜD, he is strongly involved in the matter of spinal classification according to the Medical Device Regulation (MDR).

Dr. GABRIELA SOSKUTY

Senior Vice President Global
Government Affairs & Market Access

B. Braun

Dr. EMIR OSMANAGIC

Senior Director  of Enabling Technologies
Johnson&Johnson/
DePuy Synthes

JUDITH HARGREAVES

Director

Health Economics & Reimbursement
Acelity

CONFERENCE TOPICS

DAY ONE 

  • Co-creation of successful health technologies in the context of an increasing demand, less resources and stricter regulations

  • The Impact of Medical Devices on Healthcare

  • What to Expect from the Medical Device Regulation and In-Vitro Diagnostic Regulation (MDR & IVDR)

  • Benefits of Simulation-based Medical Training

  • Access to Digital Health in Germany

  • An Impact of GDPR and other initiatives to Healthcare Industry

  • How to boost world-wide Medical Device Business using innovative regulatory initiatives

  • Why Medical Device industry needs HEMA

  • Value-added relationships with HCPs / HCOs in changing Medical Devices environment

  • Global expectations, and trends in Innovative Approaches to RWE. How to increase market accessibility and global outcomes in the face of higher public and regulatory scrutiny?

DAY TWO

  • How SaaS Business model can affect the future of Healthcare

  • Artificial Intelligence in Medical Devices

  • Using large data sets and artificial intelligence to predict outcomes and optimise service design

  • Market access in the product development process

  • How to Chase Intensive Technology Changes

  • How AI and IoT Change Everything – Disruptive Technologies in Healthcare

  • How to Leverage AI Ecosystem in Healthcare

  • R&D and Innovation in Medical Devices

  • Big data, AI-driven predictive analytics: the future of medical devices

WHO SHOULD ATTEND?

WHAT TO EXPECT

REASONS TO ATTEND

IF YOU WORK WITH MEDICAL DEVICES IN ANY CAPACITY:

  • BUSINESS DEVELOPMENT

  • COMMERCIALIZATION

  • DESIGN & DEVELOPMENT

  • DIGITAL HEALTH, AI

  • ENGINEERING

  • HEALTH ECONOMICS / MARKET ACCESS

  • INDUSTRY CONSULTANT

  • INNOVATION

  • MARKETING

  • QUALITY & REGULATORY

  • R&D

  • LEGAL & COMPLIANCE

  • PATIENT SAFETY

  • CLINICAL INFORMATION

  • WARM AND PROFESSIONAL WELCOME

  • CUTTING-EDGE TOPICS

  • WOLRD EXPERTS, THOUGHT LEADERS AND GLOBAL LEADING COMPANIESS

  • SPEAKERS FROM BOTH SIDES OF ATLANTIC

  • CONFERENCE MOBILE APPLICATION

  • PUNCTUALITY AND ATTENTION TO DETAILS

  • ENGAGING NETWORKING OVER GREAT HORS D’OEUVRES AND DRINKS

  • PROFESSIONAL, YET FRIENDLY AND RELAXED CONFERENCE ENVIRONMENT

  • PERSPECTIVES FROM DIFFERENT STAKEHOLDERS OF MEDICAL DEVICES MARKET

  • INTERACTIVE PANEL SESSIONS WITH RELEVANT TOPICS TO ENGAGE EVERYONE IN THE ROOM

  • MORE FEATURES THAN EVER!

  • MEET THE WORLD’S MARKET-LEADING MEDICAL DEVICES AND HEALTHCARE/MEDTECH COMPANIES

  • FIND PRACTICAL SOLUTIONS FOR CHALLENGES YOUR ORGANIZATION IS FACING

  • A COLLABORATIVE PLATFORM TO SHARE KNOW-HOW AMONG MAJOR MARKET PLAYERS

  • LISTEN TO THE BEST-PRACTICE EXAMPLES AND THE LESSONS LEARNED FROM THE CASE STUDIES

  • GROW YOUR PROFESSIONAL NETWORK, AND DISCUSS POTENTIAL ALLIANCES WITH THE INDUSTRY PEERS

  • GAIN A COMPETITIVE ADVANTAGE IN A RAPIDLY CHANGING BUSINESS ENVIRONMENT

  • INFLUENCE AND HELP SHAPE FUTURE TRENDS IN THE SECTOR

CHILL

SMILE

CHAT

STUDY

NETWORK

DISCUSS

LOOKING FORWARD TO SEE YOU IN AMSTERDAM!

HOME

ABOUT US

   SAMTEK GROUP

   OUR MISSION

CONFERENCES

   UPCOMING EVENTS

   PAST EVENTS

CAREERS

CONTACT US 

 

Site Map

Head Office

Edutech SRO

Krizikova 53/52,

18600, Prague

Czech Republic

 

ID: 29057647

VAT: CZ 29057647 

© 2010-2019 Edutech SRO All Rights Reserved