Global Site Selection Header

全球治疗效验实施设施之选定、可实现的评估、业务、设施管理

COUNTRY SELECTION, SITE SELECTION AND STUDY PLANNING CONSIDERATIONS
-国家选定、治疗效验实施设施选定和治疗效验计划检讨-

Optimizing Protocol Development and Site Selection: Getting it Right in the Beginning

Joseph Kim, M.B.A., Clinical Operations Director, Shire

Driving Innovation in Study Start-Up: Optimizing Site Performance through Evidence-Based Site Selection

Daphne Van, Global Trial Optimisation Manager, Centre for Project & Study Excellence, GlaxoSmithKline

Co-Presentation

Modeling the Country and Site Selection for Shortening the Clinical Development Timeline

Feng Li, Manager, Stakeholders Office, sanofi-aventis

Jaap Hoek, Vice President, Clinical Sciences & Operations, sanofi-aventis

OPTIMIZING THE FEASIBILITY PROCESS
-可实现评价过程最适化-

Importance of Site Feasibility Process: First Critical Step to a Successful Study Outcome

Sudeesh Tantry, Ph.D., Associate Director, Clinical Research, Teva Branded Pharmaceutical Products R&D, Inc.

Co-Presentation

A Collaborative Approach Looking at Feasibility: Plans to Reduce Time, Cost and Percentage of Non-Active Sites from Both the Sponsor and Site Perspective

Nye Pelton, Clinical Operations Portfolio Management, (COPM)USMD, Eli Lilly

Deena Bernstein, Director, Clinical Research, Sheridan Clinical Research

OVERCOMING CHALLENGES IN CLINICAL OPERATIONS,
SITE MANAGEMENT AND RETENTION
-克服治疗效验业务、治疗效验实施设施管理及确保的课题-

Understanding and Planning for the Increased Incidence of Non-Compliant Patients, Inappropriate Patients and Financially Motivated Patients

Ellis Wilson, Senior Director, Project Coordination, AstraZeneca

Improving Performance and Relationships with International Investigative Sites: Evaluating Relationships with Sponsors and CROs and Vice Versa

Joan Chambers, COO, CenterWatch

Sponsored by
Trifecta logo
TalkTitle to Be Announced

Trifecta (Speaker to be Announced)

Improving Operational Efficiencies within the Sponsor Organization: A Device Perspective

Kathi Durdon, Manager, Clinical Operations, Welch Allyn

OPERATIONAL CHALLENGES IN PHASE IIIb-IV
-第3b相~第4相业务上的课题-

Shared Session with Managing Post-Marketing Studies (Phase IIIb-IV) and Registries

Sponsored by
bbk logo
When Enrollment is the True Priority, Which Feasibility, Site Selection and Site Support Methods Apply Equally in Registration and Post-Approval Studies?

Jaime Cohen, Strategic Planning, BBK Worldwide

Unique Challenges of Site Management, Project Management and Ops in Post-Marketing Studies

Speaker to be Announced

Sponsored by
UBC
Is There Patient Recruitment in a Post-Marketing Study?

Tess Drahzal, Associate Director, Patient and Physician Services, United BioSource Corporation (UBC)

Operational and Organizational Challenges of Post-Marketing Requirements

Speaker to be Announced

分科委员会discussion group

Interactive Breakout Discussion Groups:

Concurrent breakout discussion groups are interactive, guided discussions hosted by a facilitator or set of co-facilitators to discuss some of the more poignant questions facing the industry. Delegates will join a table of interest to them and become an active part of the discussion at hand. It is an informal, yet informative, format that allows attendees to learn from each other and make some new contacts. To get the most out of this interactive format please come prepared to: share examples from your work, vet some ideas with your peers, be a part of group interrogation and problem solving, and, most importantly, participate in active idea sharing. Topics may include:

  • Site selection and study planning considerations: Understanding regional issues, regulatory landscapes, and local ethical processes
  • Optimizing country selection: Strategies for positioning trials for success using a global footprint
  • Optimizing the site feasibility process: Improving global site feasibility assessment to identify sites that will recruit on time and within budget
  • Cost-effective techniques for finding high performing sites: High-tech and low-tech solutions to avoid uninterested and low enrolling parties
  • Overcoming challenges in clinical operations and site management: Linking sponsors, service providers and investigative sites and positioning sites for success by anticipating their needs
  • Improving operational efficiencies in Site, CRO, and sponsor interactions: Implementing strategic relationships and other forms of partnerships
  • Driving innovation in study start-up: Optimizing processes, training leaders and leveraging technology

推荐星期一下午的短期课程

Social Media and Mobile Technology in Supporting Patients in Studies and Registries
-为了在治疗效验·登记时支持接受试验者的社会媒体和行动技术-

2012 Conference At A Glance