11th Clinical Monitoring and Patient Rec

29-30 October 2025 | Barcelona Spain

11th CMPRR Summit
Patient Recruitment Retention

WHO SHOULD ATTEND

CONFERENCE BENEFITS

CMPRR Summit 29th-30th October 2025 is targeted for professionals who are always seeking for new opportunities, visionary ways of conducting performance. 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 conference is designed to provide an opportunity for clinical & medical professionals 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, study start ups, study feasibility, outsourcing strategies, delivering clinical trials to time, cost and quality standards. The two days will cover a range of challenges facing clinical professionals in the current climate, such as communication quality, role of technologies(IoT, AI etc) in Clinical Innovation, relationships with site staff, quality standards, compliance oversight, risk based and centralized monitoring, new approaches to clinical monitoring & patient engagement.

Specifically we will look at new tools and ideas to enhance recruitment and also the benefits of increasing patient involvement and engagement. Not just with input from a range of highly respected & experienced speakers but also with emerging talents/start-ups as well in this meeting promises to be an excellent development opportunity for anyone involved in clinical trials, operations and project management.

You should not miss this annual opportunity if you are - Chiefs, Directors, Heads, Senior Manager, Leaders and Executives from:

Clinical Research/ Trials
Clinical Monitoring Operations
Clinical Operations Management
Clinical Project Management
Clinical Program
Clinical Research & Development
Regulatory and Compliance
Quality Assurance
Data Management
Clinical Oversight
Patient Recruitment
Patient Advocacy & Communities
Patient Engagement, Patient Communication
eClinical
ePRO
Study Feasibility
Medical Operations
Medical Advisers
Medical Science Liaison
Strategic Marketing
TA Commercial

For group discounts and complete details contact us.

REQUEST FULL AGENDA

OVERVIEW

Opportunity to meet top expert and decision makers from Pharma, Biotech, Medical Devices, Clinical Sites and CROs industry under one Roof

Get engaged with the professionals from leading industries
20+ Keynote Sessions
5+ Workshop sessions
Round Table Discussions – Brain storming
Panel Discussions – Interact Directly with the Panellists to raise your challenges
More than 10 Case Studies presenting by the top experts from across the industry
13+ hours Networking Opportunity
Benchmarking Opportunities
One-to-one interactions
Tea/Coffee Breaks, Social Events and Cocktail Reception
.…and much more!

REQUEST FULL AGENDA

About KP-Morgan Group

KP Morgan specializes in clinical trials, SFE, commercial excellence and Healthcare innovation events, hosting events in various locations such as Canada, USA, Europe and Dubai.

KP-Morgan Conferences have provided platforms for debate across many industry sectors including: Telecommunication, banking & financial services, retail and FMCG, investments, pharmaceuticals, IT, chemical & petro chemical.

Many argue that the innovation process cannot be managed because innovation is supposed to be about creativity and cannot be predicted. We believe in KP-Morgan that Innovation is not only about being creative and inventive; innovation is a collaborative process where ideas are taken and managed through to value-adding market introduction.

The consistent high quality of our events has given rise to a reputation for excellence, ensuring that KP-Morgan conferences provide the most fertile ground for participants to gain up-to-the-minute market intelligence and invaluable opportunities to network and generate new business.

INTERESTED IN EVENT PARTNERSHIP?

AGENDA: TOPICS AT GLANCE

Keynote Presentation, Interactive Discussions, Case Studies, Brain Storming and Round Table Discussions

Study Design, Monitoring & Patient Centric Approaches

Strategic Risk Management in clinical trial
Practical Solutions to RBM Rollout
Integrating Quality Into Clinical Trials To Ensure Effective Monitoring
Beyond Monitoring your Clinical Trial: Best Practices in Applying RBQM
Quality by design: Best Practices
Inspection Readiness - Remote Inspections
Rethinking the Path to Enrollment
Evaluate changes to monitoring procedures and activities
Making the Case for more site engagement in DCTs. Not Less.
Why Simply “Identifying” potential patients that fit a clinical trial isn’t enough?
Patient Recruitment in Emerging Countries and Challenges for Global Trials
Importance of designing a recruitment strategy prior to study initiation

Understanding the Regulators’ Guidance on Intersection with Medical Technologies
Evaluate Changes to Monitoring Procedures and Activities
Demonstrating Patient Insight from an Early Stage of Drug Development
Challenges to Interpreting Patient
Reported Outcomes in Clinical Trials
Engaging stakeholders in Recruitment strategies
Patient Journey Mapping and measuring the patient experience(PEX)
Holistic Approach to Patient Recruitment
Optimize CT operations and boost site performance
Data Analytics as key pillars
Growing Involvement of Online Communities and Advocacy Groups in Patient Recruitment

PATIENT EMPOWERMENT: AS PARTER

Diversity & Inclusion Criteria
How to diversify your patient recruitment approaches
Strategic Issues in Diverse Enrollment
Complexity of Study Design and SOPs
Site Performance: Joint approach
Research-Naive Sites & Site Staff Motivation
Aspects of Informed Consent and Vulnerable Patients in CTs
Engaging Sites and Patients: Study Design
Site Selection Methodology
Quality Management & Assessment
How to retain Patients in Long-Run Trials - Case Study TAs

Overcoming major barriers to clinical trial recruitment
Strategic Issues in Diverse Enrollment Planning and Execution
Challenges for Going Global in an Increasingly Regulated World (GDPR, EMRA, CFR, etc.)
Strategic Issues in Diverse Enrollment Planning and Execution
Building your recruitment and retention strategies
Overcoming the challenges face by sites and investigators in patient retention

CLINICAL TECHNOLOGIES & TRENDS

Digital Medicine for Patient Engagement in Clinical Trials
DCTs: How to Prepare for Transformation
How Technology & Real-time Data Can Enable Recruitment Success
Role of Wearables, AIs, Digitalisation, eHealth in Patient-Centric Approaches & Clinical Innovation
Selecting Patient-Facing Technology: Why It Is Important for Patient-Centric Trials

Intersecting Digital Health and Decentralized Clinical Trial Operations for Optimal Patient Outcomes
Understanding Technology Advancement at the Patient Level
Revolutionising Clinical Trials
Clinical Innovation: What it means to patients
Understanding different aspects of AIs