The 3rd Annual Patient Recruitment and Retention Summit ASIA
IS OVER!
100+
Satisfied Delegates
TOP 20
Industry Speakers
Over 15
Experience Based Case Studies
We are looking forward to welcoming you
on board in 2017!
STAY UPDATED
Provide us with your contact details and our team will get back to you with all the updates regarding the upcoming edition of this event.
See the past Speakers and Case Studies
from Last Annual BELOW
Hiroshi
SUGII
Managing Director / Member of the Board Directors CMR Development Division
Clarence
KHOO
Associate Director, Clinical Operations
Dr.Shailendra
BAJPAI
Regional Medical Director
Dr.Shweta
UPPAL
Head – CMRQ (Singapore, Malaysia, Brunei)
Dr.Pratik
SHAH
Head- Clinical, Medical & Regulatory Affairs
Cristina
CHANG
Vice President / Medical, Clinical Development
This is the event where you can access the people and ideas that matter most to your business.
A programme that will inspire you and gives you opportunity to network with your peers on one of the most leading and exciting events.
- Networking possibilities
- Discussing key issues in breakout sessions
- Meet with new business partners
- Unrivalled speakers lineup with real industry professionals
- One-on-One Business Meetings
- Focused, productive and balanced Agenda
- Informal gatherings outside conference hours
Allan Lloyds events are famed for being highly interactive. Through our special discussion panels and roundtable discussion formats you will be able to discuss all of the complex issues that you are facing with our speakers and delegates.
PATIENT MOTIVATION & RECRUITMENT: The new patient
recruitment practices and ways to retain patients in clinical trials
COST-EFFECTIVNESS: Development of cost-effective clinical trial
infrastructure capabilities in the emerging markets
CLINICAL TRIAL FEASIBILITY: Better understanding of the trial
feasibility impact
REGULATORY ENVIROMENT: Gain better insight of the current situation
of clinical trials and regulatory environment
CLINICAL RESEARCH: How does the clinical research lead to improvements in the patient care
Members of board, C-level, Senior Vice Presidents, Vice Presidents, Directors and Heads of departments from pharmaceutical industry involved in:
- Clinical Operations
- Clinical Development
- Patient Recruitment and Retention
- Clinical Research
- Clinical Site Management
- Global Monitoring Operations
- Drug Safety and Development
- Scientific Affairs
Ultimate Session
FOR NETWORKING
Every morning starts with a great ice-breaking activity – Speed Networking Session. This session is designed to give all participants the opportunity to meet and introduce themselves to their fellow participants before the official conference starts.
Don’t forget your business cards!
Provided Networking Sessions include Coffee Breaks, Networking Lunches, a Cocktail Reception, plus informal gatherings outside conference hours –key tools for establishing future business connections with fellow industry peers.
Interesting Case Studies from the Agenda 2016
RECRUITMENT AND RETENTION OF PATIENTS IN JAPAN
Hiroshi
SUGII
Managing Director / Member of the Board Directors CMR Development Division
How to recruit and retain a patient in the big scale of pivotal clinical trial in Japan and Asia by ensuring the productivity optimization?
Recently it has been very challenging for pharmaceutical company to recruit enough patients in a balancing speed, cost and quality for the case of clinical trials in the chronic disease area in Japan because the clinical trial scheme would become complicated and competitive. I would take an example of diabetes drug development and issues of how to proceed the effective clinical trials by mitigating the issues and risks. Key words are: 1) optimal planning, 2) globalization, 3) incentive scheme from my perspective.
- Introduction
- Current situation of clinical trials and regulatory environment
- Productivity improvement and Key talent development in clinical operations are the key to success
- Optimal development model by examples
- Issue and countermeasure
- Conclusion
CLINICAL TRIAL FEASIBILITY
Dr.Cristina K.
CHANG
Vice President / Medical, Clinical Development
The significant importance of Clinical trial Feasibility
Clinical trial conduction requires a lot of commitment and resources allocation and its smooth conduction to impact hugely on the success of a compound. Time spent for the clinical trial is critical and one element that affects it is the good feasibility done before starting it.
- What is the impact of trial feasibility?
- What is the due diligence for feasibility?
- How to identify the best sites and best patient pool?
We are looking forward to welcoming you
on board in 2017!
PATIENT RETENTION IN CLINICAL TRIAL
Dr. Pratik
SHAH
Head- Clinical, Medical & Regulatory Affairs
Plan to improve patient retention in clinical trial
• Current strategies used to improve patient retention
• Brief about new ways to improve patient retention
• Role of traditional strategies
Pre-Conference Workshop
Site Selection and its Requirements
- What are the key requirements for the site selection?
- What is the right time to select a site for the clinical trial?
- What is the connection between a successful site selection
and a recruitment of the right patient? - What has to be considered when selecting the site?
- Are pharmaceutical companies capable of improving the site
selection?
Funding and Reimbursement of the Clinical Trials
- Who is the main source for funding the clinical research?
- What are the main costs for the patients?
- What are the ways to minimize the costs?
- Introduce some possible cost saving strategies
Sponsors 2016
We are looking forward to welcoming you
on board in 2017!
STAY UPDATED
Provide us with your contact details and our team will get back to you with all the updates regarding the upcoming edition of this event.