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: CRA Experience and Effectiveness – Training Alternatives Session
Session 5: Patient Centric Payments in Clinical Trials
Session 6: Patient Reimbursements Challenges

Session 7: Risk based and Centralized Monitoring
Session 8: Remote Monitoring for CT
Session 9: Communication and transparency with clinical sites about Risk Based Monitoring(RBM)
Session 10: Risk assessment and management
Session 11: Mitigating the challenges of CT Monitoring Shifting Monitoring
Session 12: Site Selection, Start-up & Activation Study Feasibility
Session 13: Relationship between Sites, CRO, Patients, investigators & Clinical Trial Teams
Session 14: Changing Roles of Clinical Project Managers
Session 15: Big Data – CT Data Management
Session 16: Trends in the globalization of clinical trials

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: How to retain Patient in long run trials
Session 6: Patient Centricity and Patient Empowerment
Session 7: e-Patient Recruitment in Emerging Markets
Session 8: Patient Recruitment: Sites key to patient search
Session 9: Multi-Channel Patient Recruitment
Session 10: Biosimilar Trials: Detecting and Eradicating Barriers to Patient recruitment
Session 11: Use of smartphone apps to Recruit & Retain patients
Session 12: Patient Recruitment in Emerging countries and Challenges for Global Trials
Session 13: Site-specific recruitment plans
Session 14: Clinical Enrollment Manager programs

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

1. Who should attend?
You should not miss this annual opportunity if you are – Chiefs, Vice Presidents, Directors, Heads, Leaders, Managers and Associates from:
Clinical Research Associate:
  • Clinical Trials
  • Clinical Monitoring Operations
  • Clinical Operations Management
  • Clinical Project Management
  • Clinical Program
  • Clinical Research
  • Clinical Development
  • Regulatory and Compliance
  • Quality Assurance
  • Data Management
  • Clinical Oversight
  • Patient Recruitment
  • Patient Officer
  • Patient Advocacy
  • Patient Engagement
  • Patient Communities
  • eClinical
  • Strategic Marketing
  • Study and Feasibility Management
  • Medical Operations
  • Medical Advisers
  • Medical Science Liaison
2. Where will the CMPRR Conference take place?
3. How do I register for the event?
4. What would be the conference layout?
5. My company/organization is interested in exhibiting at the CMPRR conference and/or sponsoring the conference. Who should I contact?

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



Overall Participants


Case Studies


Companies Enrolled


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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Submit - CMPRR Summit Amsterdam Netherlands November 2016

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