Revolutionize Your Clinical Trials with Smart, Next-Gen Virtual Strategies!
Date: July 18, 2025
Duration: 6 Hours
Time: Starts at 10 AM EST
Are you ready to elevate your clinical trial process with the power of smart trials? This one-day virtual program is your gateway to transforming how trials are conducted. Imagine cutting timelines, slashing costs, and driving incredible ROI with advanced virtual tools, data-driven methodologies, and streamlined operations! This program will take you from traditional trial challenges to a smart, virtual-first strategy that amplifies results and redefines success.
Facing Conventional Roadblocks? Smart Trials Have the Answers!
Starting or managing a clinical trial often feels like navigating a maze—from regulatory hurdles, site management, and patient recruitment to data accuracy, budget constraints, and compliance. These challenges are real, but smart trials offer breakthrough solutions by transforming each stage of your trial into an efficient, seamless experience. Imagine trials that are faster, safer, and easier to manage! With AI-driven recruitment, remote patient monitoring, and real-time data accuracy, smart trials are revolutionizing the industry.
Your Guide: Dr. Mukesh Kumar
With a track record of over 20 successful clinical trials and hundreds more supported in advisory roles, Dr. Mukesh Kumar will share how to bridge the gap between traditional and smart trials. Through hands-on insights, compelling case studies, and engaging sessions, he’ll reveal how innovative tools like remote monitoring, digital data capture, and real-time analytics are taking trials to new heights—making high-efficiency and low-cost trials the new standard.
What You’ll Experience:
This isn’t just a learning event; it’s an empowering transformation, offering practical, strategic guidance grounded in two decades of experience. By combining conventional trial expertise with breakthrough smart technologies, you’ll walk away with the tools to take control of your clinical trials, speed up recruitment, achieve flawless data quality, reduce timelines, and control your trial’s costs in ways you never thought possible!
Speaker: Mukesh Kumar
PhD, RAC | CEO, FDAMap
For more info, fill the box below. We will contact you within 24 hrs.
Foundations of Virtual Clinical Trials
Objective: Gain a comprehensive understanding of the fundamental principles and key considerations in virtual clinical trial design.
Lesson 1: Introduction to Virtual Clinical Trials
- Overview of virtual clinical trials and their benefits
- Comparison with traditional clinical trials
- Regulatory landscape and guidelines
Lesson 2: Virtual Trial Design and Planning
- Protocol development for virtual trials
- Selection of appropriate technologies and platforms
- Ethical considerations and participant protection
Participant Recruitment and Engagement
Objective: Learn effective strategies for recruiting and engaging participants in virtual clinical trials.
Lesson 3: Participant Recruitment Strategies
- Targeted recruitment approaches
- Informed consent in virtual trials
- Overcoming barriers to enrollment
Lesson 4: Participant Engagement and Retention
- Building rapport and trust remotely
- Enhancing participant compliance and follow-up
- Managing participant expectations and concerns
Data Collection and Management in Virtual Trials
Objective: Explore remote data collection methods, tools, and best practices for ensuring data integrity and privacy.
Lesson 5: Remote Data Collection Methods
- Electronic data capture (EDC) systems
- Wearable devices and remote monitoring
- Patient-reported outcomes (PROs) and e-diaries
Lesson 6: Data Integrity and Privacy
- Ensuring data quality and accuracy
- Data privacy and security considerations
- Remote monitoring and oversigh
Regulatory Compliance and Ethical Considerations
Objective: Understand the regulatory and ethical requirements specific to virtual clinical trials and learn strategies for ensuring compliance.
Lesson 7: Regulatory Considerations
- FDA guidelines and regulatory framework
- Institutional Review Board (IRB) approvals
- Informed consent process and documentation
Lesson 8: Ethical Challenges and Solutions
- Balancing participant autonomy and remote oversight
- Ensuring equity and diversity in virtual trials
- Addressing potential biases and limitations
Implementing and Managing Virtual Trials
Objective: Develop practical skills for successfully implementing and managing virtual clinical trials
Lesson 9: Trial Execution and Site Management
- Remote site selection and training
- Ensuring compliance and adherence
- Remote monitoring and support
Lesson 10: Data Analysis and Reporting
- Statistical considerations in virtual trials
- Analysis of remote data and endpoints
- Preparation and submission of trial results
Register Online (By clicking on the links below)
Prices are in US Dollars.
The registration fee includes the workshop and all related course materials.
Terms & Conditions to register for the Workshop
Your Registration for the workshop is subject to following terms and conditions. If you need any clarification before registering for this seminar, please email us at info@fdamap.com
Payment:
We accept credit card, debit card, and PayPal.
Cancellations and Substitutions:
Written cancellations through fax or email (from the person who has registered for this conference) received at least 20 working days prior to the start date of the event will receive a refund — less a $200 administration fee per person. No cancellations will be accepted — nor refunds issued — within 20 working days from the start date of the event.
On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($200) will be transferred to any future FDA Map event and a credit note will be issued.
