£1,404.95 – £4,944.95

2nd European Clinical Quality Oversight Forum (exl) AS

Event Information

Share this event

Date and Time

Location

Location

London

London

United Kingdom

View Map

Refund Policy

Refund Policy

No Refunds

Friends Who Are Going
Event description

Description

2nd European Clinical Quality Oversight Forum

Our inaugural European CQOF in 2016 attracted 100 clinical quality experts, with over 70% representing more than 45 different pharmaceutical, biotechnology, and medical device companies from all over the world. We are pleased to announce our 2nd European Clinical Quality Oversight Forum, taking place 26–27 February 2018 again in London. This interactive event focuses on ensuring trial integrity by effectively assessing, optimising and managing the quality of clinical vendors and sites and attracts 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 optimising your company’s clinical vendor and site oversight approach.

Top Five Reasons to Attend

  1. Learn from the industry’s leading clinical operations and quality experts from around the globe, as they candidly share their experiences, strategies and guidance for selecting and managing your clinical partners to ensure compliance and maximise performance
  2. Benchmark your clinical quality oversight strategy against other similar-sized companies to ensure your approach is optimal and effective
  3. Stay current on the changing GCP global regulatory environment and the impact on clinical compliance, quality, and operations
  4. Integrate a risk-based, resource-optimizing approach for effective selection, monitoring and long-term management of your clinical vendors and sites
  5. Position your trial for success by ensuring your clinical vendors and sites are inspection ready with the latest tools, technologies, and audit strategies
2016 Audience Demographics74% Pharmaceutical, Biotechnologyand Medical Device Companies74% Pharmaceutical, Biotechnologyand Medical Device Companies24% Clinical Service Providers24% Clinical Service Providers2% Other2% OtherHighcharts.com

60% Represented Director-Level and Above

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
  • 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


Agenda

Topics we are considering for this year’s programme include:

  • Interpreting and Aligning with ICH E6 R2
  • Reviewing your Trial Master File from the EMA Perspective
  • Achieving a Confident State of Inspection Readiness
  • Examining the Progress and Impact of Inspection Collaboration Across FDA, EMA and PDMA
  • Assessing the Impact of Brexit on Clinical Compliance and Operations
  • Effectively Overseeing CRO Monitoring “Monitoring the Monitors”
  • Optimising Data Integrity through Effective Oversight
  • Identifying Strategic Clinical Vendors
  • Measuring the Clinical Quality of your Partners
  • Managing Quality between Sponsors and CROs
  • Initiating a Quality by Design Approach
  • Evaluating Quality and Oversight Concerns Specific to China
  • Prioritising Data Quality to Proactively Identify Possible Noncompliance
  • Overcoming Global Compliance Challenges
  • Developing a Risk-Based Vendor and Site Audit Strategy
  • Executing Effective Risk-Based Monitoring

Please contact the event manager Marilyn below for the following:
- Discounts for registering 5 or more participants.
- If you company requires a price quotation.
Event Manager Contact: marilyn.b.turner(at)nyeventslist.com
You can also contact us if you require a visa invitation letter, after ticket purchase.
We can also provide a certificate of completion for this event if required.

NO REFUNDS ALLOWED ON REGISTRATIONS
-----------------------------------------------------------------
This Event Listing is Promoted by
New York Media Technologies LLC in association
with EXL Events Inc
http://www.NyEventsList.com
http://www.BostonEventsList.com
http://www.SFBayEventsList.com
-----------------------------------------------------------------
MYL170801CEV MAR170926UPT

Share with friends

Date and Time

Location

London

London

United Kingdom

View Map

Refund Policy

No Refunds

Save This Event

Event Saved