How to Start a New Clinic as a Trial Site
Date: May 23, 2025
Duration: 60 Minutes
Time: 12 PM EST
Why should I attend:
- Learn the Value of Certification: Certification in clinical trials is the cornerstone of success for any investigator. It ensures regulatory compliance, ethical conduct, and the delivery of high-quality clinical trial outcomes.
- Gain Invaluable Experience: The key to becoming a sought-after investigator lies in gaining relevant experience in clinical research. We will equip you with essential tips on how to become a sub-investigator, allowing you to shadow experienced Principal Investigators in real clinical trial settings. This hands-on experience will be invaluable in your journey to becoming a successful clinical researcher.
- Fund your Clinical Research Facility: Starting a private clinical research facility requires funding, and we will show you the best practices to acquire the financial support you need. Our seminar will also guide you in choosing the ideal location and size for your facility, tailored to the phase of testing you’re interested in performing.
- Create a Solid Infrastructure: A successful clinical trial site thrives on a solid infrastructure. We will walk you through the essential considerations for informed consent, safety and deviation reporting, and study drug administration and destruction. By the end of the seminar, you will be well-prepared to establish an efficient and compliant clinical research facility.
- Build a Stellar Team: Your team is the backbone of your clinical trial site. We’ll provide you with valuable insights on hiring the right staff, ensuring you have a competent and dedicated team to support your research endeavors.
Don’t miss this golden opportunity to turn your passion for medical research into a thriving career. Join us at our seminar and unlock the door to a world of possibilities in clinical trials.
Secure your spot now and take the first step towards a rewarding future in clinical research. Sign up for our “How to Start a New Clinic as a Trial Site” seminar today!
- Regulatory affairs professionals
- Physicians and Specialists
- Clinical Researchers
- Clinic Administrators and Managers
- Research Coordinators and Site Managers
- Clinical Trial Professionals
- Project Managers and Clinical trial specialists
- Academic Institutions and Research Organizations
- Healthcare Entrepreneurs
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
We accept credit card, debit card, and PayPal.
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.
