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7th Annual European Medical Device Clinical Research Conference
Our Price:
$
395.00
Product Code:
2208
Qty:
Product Info
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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