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7th Annual European Medical Device Clinical Research Conference



 
Our Price: $395.00

Product Code: 2208
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Building on the success of the previous editions of the EU Medical Device Clinical Research conference, the 2014 program provides a platform for knowledge share and peer to peer education through highly practical case studies and best practices focusing on optimizing clinical research operations, notably in light of data generation and utilization for technical reviews, publishing or reimbursement needs. Innovative strategies to achieve site selection and patient enrollment goals will also be thoroughly examined alongside impactful methods to successfully complete clinical trials in a time and budget friendly fashion.


KEY DIFFERENTIATORS

  • New high level topics:
    • Clinical Excellence Leading to Commercial Excellence
    • Study Design
    • Maximizing Data Generation and Utilization
    • Budgeting Trials
    • Hungarian Proactive Clinical Regulation
    • CRO Selection
    • Remote Monitoring
    • Biostatistics
    • Clinical Trials in China


PRODUCT INFORMATION:
Presentations slides are in PDF. format
All files are available for immediate download.


INCLUDES THESE PRESENTATIONS:


OPTIMIZING TEAM COLLABORATIONS IN THE DEVICE CORPORATION TO STREAMLINE OPERATIONS
Ihsen Merioua, Director of THV Clinical Programs
EDWARDS LIFESCIENCES

MDR DEVELOPMENTS: NEW CLINICAL RESEARCH REQUIREMENTS
Maria Palka-Santini, Head of Clinical Research & Health Economics
3M CRITICAL AND CHRONIC CARE

CE MARKING - CHANGING AND EVOLVING REQUIREMENTS

Gert Bos, Head of Regulatory and Clinical Affairs
BSI

HOW THE EXISTING HUNGARIAN CLINICAL REGULATION FULFILLS FUTURE MDR MEASURES
Péter Bunyitai, Head of Department, Medical Devices
EEKH - OFFICE OF HEALTH AUTHORIZATION AND ADMINISTRATIVE PROCEDURES, HUNGARY

STUDY TYPES AND UNDERLYING OPPORTUNITIES
Hindrik Robbe, VP Field Clinical Affairs EMEA
ST JUDE MEDICAL

INTEGRATING REIMBURSEMENT AND HEALTH ECONOMICS IN CLINICAL EVIDENCE STRATEGY

Amit Kukreja, Director of Market Access – EMEA
SECOND SIGHT MEDICAL PRODUCTS

SECURING PROTOCOL ADHERENCE AND REDUCING TIMELINES VIA HCP TRAINING AND CONTINUOUS SUPPORT
Edo Knijff, Manager, Clinical Affairs
ORTHOFIX

OVERCOMING EVOLVING PATIENT RECRUITMENT AND RETENTION CHALLENGES

Cristina Rubiolo, Team Leader, Emerging Applications Clinical Research
MED-EL

CLINICAL STUDY RISK-BASED MONITORING: OPPORTUNITIES AND REGULATORY ACCEPTANCE

Vytis Jusevicius, Project Director, Project Management
APTIV SOLUTIONS, AN ICON PLC COMPANY

CASE STUDY: PROS & CONS OF CLINICAL STUDY REMOTE MONITORING

Kirsten Welz, Senior Medical Research Manager
NAMSA

HOW BIOSTATISTICS IMPACT CLINICAL STUDY DEVELOPMENT AND MANAGEMENT
Georgeta Natasa Forte, Vice President, Clinical & Scientific Affairs
SPINEART

CASE STUDY : CLINICAL TRIAL FOR CLASS III MEDICAL DEVICES IN CHINA
Alexandra Baer, Senior Regulatory Affairs Executive
CROMA PHARMA

Arkan Zwick, Director Regulatory Affairs & Legal
CROMA PHARMA


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