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Clinical Quality Oversight Forum 2018 Philadelphia

Wed, October 10 - Fri, October 12, 2018 Philadelphia, Pennsylvania
Sonesta Philadelphia Downtown Rittenhouse Square 1800 Market St Philadelphia, Pennsylvania 19103 United States +1 215-561-7500

About Clinical Quality Oversight Forum 2018 Philadelphia

CLINICAL QUALITY OVERSIGHT FORUM, PHILADELPHIA, OCTOBER 10-12, 2018

ExL’s 9th Clinical Quality Oversight Forum focuses on ensuring trial integrity by effectively assessing, optimizing and managing the quality of clinical vendors and sites. This forum acts as the annual gathering for clinical quality, operations, management and audit professionals to engage and candidly share their experiences, struggles, obstacles, and achievements when working with varying clinical partners including CROs and investigator sites. Learn from this experienced group and take away proven, results-driven, risk-based strategies for optimizing your company’s clinical vendor and site oversight approach.

This event will take place at Sonesta Philadelphia Downtown Rittenhouse Square, 1800 Market St, Philadelphia, Pennsylvania.

Who Should Attend?

This event is designed for professionals from pharmaceutical, biotechnology and medical device companies; CROs; and other clinical service providers who have responsibilities in the following areas:

  • Quality Management/Clinical Quality Management
  • Clinical Quality Assurance/QA/CQA
  • Clinical Quality Control/QC/CQC
  • Clinical Operations/Management/Research/Development
  • Compliance/Clinical Compliance/Regulatory Compliance
  • Monitoring/Site Management/Study Management
  • Clinical Outsourcing/Vendor Management/Third Party Management
  • Good Clinical Practice/GCP
  • Auditing/Auditor
  • Clinical Risk/Risk Assessment
  • Regulatory Affairs
  • Medical Affairs

The event is also of interest to:

  • Investigative Sites
  •  Academic Research Organizations
  • Central, Imaging and ECG Labs
  •  IVRS Companies
  • EDC Companies
  • Other Clinical Service Providers

About Clinical Quality Oversight Forum 2017

CLINICAL QUALITY OVERSIGHT FORUM, OCTOBER 11-13, 2017

What is this event?

8th Clinical Quality Oversight Forum will be focusing on ensuring trial integrity by effectively assessing, optimizing and managing the quality of clinical vendors and sites.

This forum acts as the annual gathering for clinical quality, operations, management and audit professionals to engage and candidly share their experiences, struggles, obstacles, and achievements when working with varying clinical partners, including CROs and investigator sites.

It’s an unrivalled opportunity to learn from this experienced group and take away proven, results-driven, risk-based strategies for optimizing your company’s clinical vendor and site oversight approach.

Where is this event located?

This event will take place at Sheraton Philadelphia Downtown Hotel, 201 N 17th St, Philadelphia, Pennsylvania, USA.

Who should attend this event?

This conference is designed for professionals from pharmaceutical, biotechnology and medical device companies; CROs; and other clinical trial service providers whose responsibilities involve the following:

  • Quality Management/Clinical Quality Management
  • Clinical Quality Assurance/QA/CQA
  • Clinical Quality Control/QC/CQC
  • Clinical Operations/Management/Research/Development
  • Compliance/Clinical Compliance/Regulatory Compliance
  • Monitoring/Site Management/Study Management
  • Clinical Outsourcing/Vendor Management/Third-Party Management
  • Good Clinical Practice/GCP
  • Auditing
  • Clinical Risk/Risk Assessment
  • Regulatory Affairs
  • Medical Affairs

What are some highlights of this event?

Event Highlights:

  • CHAIRPERSON’S WELCOME AND INDUSTRY UPDATE
  • Examining Effective Approaches for Building and Growing a Corporate Quality Culture and the Realized Benefits
  • Examining How Vendor Oversight and Outsourcing Models Are Changing as a Result of ICH E6 R2
  • Developing an Effective Preparation Plan That Guides All Stakeholders to Achieve Inspection Readiness While Managing the Clinical Trial
  • Building Inspection Readiness as a State, Not a Process, and How to Get There
  • Leveraging the TMF As an Oversight Tool to Proactively Identify RiskDefining the Roles of QA and Clinical Teams and Recognizing When Collaboration Is Productive or Independence Must Be Maintained
  • Identifying and Discussing the Top Challenges, Concerns and Obstacles Relating to Effective Clinical Quality Oversight

Speakers:

  • Catherine Arthey
  • Bob Castellucci
  • Katie Delaney, DHA
  • Cheryle Evans
  • Kristy Galante, M.S.
  • Duncan Hall
  • Paul Houri
  • Prajna Kumar, Ph.D.
  • Crissy MacDonald, Ph.D.
  • Armelde Pitre

Why should I attend this event?

By attending this event you will be:

  • Identifying Key Risk Indicators during Vendor Selection and Qualification to Ensure the Right Partner is Chosen.
  • Developing a Risk-Based Auditing Approach to Proactively Assess Risk and Optimize Resources.
  • Ensuring a Shared Concept of Quality amongst Partners with an Effective Quality Agreement.

 

 

 

About 7th Clinical Quality Oversight Forum

7TH CLINICAL QUALITY OVERSIGHT FORUM, OCTOBER 17-19, 2016 WHAT IS CLINICAL QUALITY OVERSIGHT FORUM? 7th Clinical Quality Oversight Forum, taking place October 17-19 in Philadelphia, acts as the annual gathering for clinical quality, operations, management and audit professionals to engage and candidly share their experiences managing the quality and productivity of clinical partners. Learn from this experienced group and take away proven results-driven, risk-based strategies for optimizing your company’s clinical vendor and site oversight approach. WHERE IS CLINICAL QUALITY OVERSIGHT FORUM LOCATED? The forum is held at Hilton Philadelphia at Penn’s Landing , 201 South Columbus Blvd, .Philadelphia, Pennsylvania. WHO ATTENDS CLINICAL QUALITY OVERSIGHT FORUM ? This event is designed for professionals from pharmaceutical, biotechnology and medical device companies; CROs; and other clinical service providers who have responsibilities in the following areas:
  • Quality Management/Clinical Quality Management
  • Clinical Quality Assurance/QA/CQA
  • Clinical Quality Control/QC/CQC
  • Quality Operations/Quality Systems/Quality Processes
  • Management/Clinical Operations/Research/Development
  • Compliance/Clinical Compliance/Regulatory Compliance
  • Clinical Outsourcing/Vendor Oversight and Management/Strategic Partnerships/Third-Party Management and Oversight
  • Clinical Risk/Quality Risk/Risk Assessment/Risk Management
  • Site Monitoring/Site Management/Study Management/Trial Management
  • Good Clinical Practice/GCP
  • Auditing
  • Inspection/Inspection Readiness
  • Clinical Data
  • Regulatory Affairs
WHAT IS CLINICAL QUALITY OVERSIGHT FORUM ALL ABOUT? Clinical quality oversight forum is focuses on ensuring trial integrity by effectively assessing, optimizing and managing the quality of clinical vendors and sites. This forum acts as the annual gathering for clinical quality, operations, management and audit professionals to engage and candidly share their experiences, struggles, obstacles and achievements when working with varying clinical partners, including CROs and investigator sites. Learn from this experienced group and take away proven, results-driven, risk-based strategies for optimizing your company’s clinical vendor and site oversight approach. WHY SHOULD I ATTEND CLINICAL QUALITY OVERSIGHT FORUM? 1. Learn from the industry’s leading clinical operations and quality experts as they candidly share their experiences, strategies and guidance for selecting and managing your clinical partners to ensure compliance and maximum performance. 2. Benchmark your clinical quality oversight strategy against other similar-sized companies to ensure your approach is optimal and effective. 3. Integrate risk-based approaches for effectively selecting, monitoring and managing your clinical vendors and sites — while optimizing your resources. 4. Position your trial for success by ensuring your clinical vendors and sites are inspection ready with the latest tools, technologies and audit strategies. 5. Design your own agenda and choose your preferred learning environment with the selection of interactive workshops, session tracks, educational presentations, dynamic panels, interactive roundtables and ample networking opportunities  

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