Event Schedule

1st DAY

Session 1: Identifying Challenges and managing risk
Session 2: Sponsor monitoring SOP
Session 3: Clinical Trial Protocols and Protocol Compliance Improvement
Session 4: Quality Assurance
Session 5: CRA Experience and Effectiveness – Training Alternatives

2nd DAY

Session 1: Digital Evolution – New ways to achieve digital excellence
Session 2: Importance of Patient Centricity in Clinical Trials
Session 3: Communication between stakeholders
Session 4: How to optimize patient recruitment
Session 5: Patient Centricity
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About Event

CMPRR Summit Overview:

Monitoring is key to the success of clinical trials and the role of the monitor is varied and ever-changing. Ensuring monitoring meets the key objectives regarding subject safety and data quality requires a range of skills, knowledge and experience. This meeting is designed to provide an opportunity for monitors to develop and hone skills and knowledge, share experiences and learn from each other thus enabling them to improve their performance and ultimately to play their part in delivering clinical trials to time, cost and quality standards. The first day will cover a range of challenges facing monitors in the current climate, such as relationships with site staff, quality standards, risk based and centralized monitoring and changing technology. The second day will focus on the key area of subject recruitment and retention. Specifically we will look at new tools and ideas to enhance recruitment and retention and also the benefits of increasing patient involvement and engagement. With input from a range of highly respected and experienced speakers this meeting promises to be an excellent development opportunity for anyone involved in monitoring clinical.

Frequently asked questions

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Pricing for Ticket

    • 1. BASIC

        • Entry to conference
        • -
        • Business Lunch
        • Tea and snacks
        • Cocktail Reception
    • register now
    • 2. PREMIUM

      • Entry to conference
      • One complimentary pass
      • Business Lunch
      • Tea and snacks
      • Cocktail Reception
    • register now
    • 3. GOLD

      • Entry to conference
      • Accommodation at venue
      • Business Lunch
      • Tea and snacks
      • Cocktail Reception
    • register now
20

Sessions

100

Overall Participants

20

Case Studies

80

Companies Enrolled

Speakers

Ilaria Di Resta

Ilaria Di Resta

Global Start Up Project Manager, Covance Read More
Jo Burmester

Jo Burmester

Head of Global Operations, PharmaSchool / Editor, The Journal of Clinical Research & GCP Read More
Kai Langel

Kai Langel

Co-Founder & Director, Patient Solutions, eClinicalHealth Read More
Lisa Hellström

Lisa Hellström

Clinical Study Manager, Lundbeck Read More
Loreto Taboada

Loreto Taboada

International Clinical Operations Department Manager, Servier Read More
Lydia Dorrego

Lydia Dorrego

Country Study Manager for Global Studies, IBD and Oncology diseases, Roche Read More
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