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)

Single

Individual

$ 599

Corporate

5 People

$ 2099

Corporate

10 People

$ 3099

​​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.

For more info, fill the box below. We will contact you within 24 hrs.