5 Steps to Finding the Best Sites for Your Clinical Trial
Date: June 16, 2025
Duration: 60 Minutes
Time: 12 PM EST
This webinar, presented by a leading clinical trial expert, will discuss best practices for clinical site feasibility. Common errors in site selection and potential solutions will be discussed. The seminar will highlight key areas that should be covered in the site feasibility analysis, along with tips for adjustments to fit the desired sites. Best practices for incorporating factors governing selection of sites such as sponsor preferences, site and PI visibility, subject matter expert opinions, past history, publicly available information on past performance, financial and logistical considerations and many other factors will be discussed. The seminar will highlight key regulatory requirements, dos and don’ts, common areas of concern, and trouble-shooting practices for FDA regulated industry using case studies and examples from the presenter’s vast experience helping companies big and small find good clinical sites. The webinar will provide precise and complete list of measures and components of checklists to be implemented by sponsors to bullet-proof their site selection.
- Best practices for site selection
- Similarity and differences in trials for drugs, biologics and medical devices
- How to best use the subject matter expert opinion for site selection
- Pros and cons of using “famous” sites in your study
- Ways to use new and inexperienced sites
- Risk-based site selection
- Strategies for findings the best sites for your trials
- Clinical research associates
- Clinical project managers
- Sponsors
- Regulatory affairs personnel
- Quality assurance personnel
- Vice presidents, Directors and Managers
- People interested in investing in the FDA-regulated industry
Speaker: Mukesh Kumar
PhD, RAC | CEO, FDAMap
For more info, fill the box below. We will contact you within 24 hrs.
Webinar Fee
Prices are in US Dollars.
The registration fee includes: The live webinar & all related course materials.
Terms & Conditions to register for the Webinar
Your Registration for the workshop is subject to following terms and conditions. If you need any clarification before registering for this webinar please email us at info@fdamap.com
Payment
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Cancellations & Substitutions:
Written cancellations through fax or email (from the person who has registered for this conference) received at least 5 business days prior to the start date of the event will receive a refund — less a $30 administration fee. No cancellations will be accepted — nor refunds issued — within 5 business days before the start date of the event. You may however, choose to substitute the webinar for which you are registered with some other webinar in the future.
On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($30) will be transferred to any future FDA Map event and a credit note will be issued. No-shows will be charged the full amount.
Webinar material will be uploaded on the website 24 hours before the scheduled date of the webinar. In case it is not available on the website due to some technical issues, we will email the material a few hours before the start of the webinar.
In the event FDA Map cancels the webinar, FDA Map will issue a full refund to all the registrants for that webinar. Some topics and speakers may be subject to change without notice.
