HIPAA Training and Certification for Clinical Trial Professionals: What Applies, What Doesn’t
Date: April 28, 2025
Duration: 60 Minutes
Time: 12 PM EST
Why should I attend:
1. Empowerment through Knowledge: In the realm of clinical trials, understanding the HIPAA Privacy Rule is paramount. Our workshop is designed to equip you with a clear and concise understanding of the rules governing the protection of human subjects in research. Gain valuable insights into the scope, key terms, components, principles, and core elements of HIPAA, so you can confidently navigate the intricacies of the law.
2. Extensive Coverage: Don’t let uncertainty cloud your judgment when dealing with sensitive patient information. Our workshop will delve into the specifics of who and what is covered under HIPAA, ensuring you know precisely how to handle patient data with the utmost care and confidentiality.
3. Champion Patient Rights: HIPAA is not just a set of rules; it represents a commitment to preserving patient rights. Learn about the patient rights mandated by HIPAA and how to respect and uphold them while conducting clinical trials and medical research.
4. Research Disclosures Made Clear: Navigating research disclosures under the HIPAA Privacy Rule can be challenging. Our workshop will shed light on the nuances of HIPAA Authorization and Waiver of Authorization, helping you make informed decisions that balance research needs with privacy concerns.
5. Spot and Prevent Common Violations: Stay ahead of the curve by understanding the common violations that occur in the context of HIPAA. Our workshop will guide you on how to avoid these pitfalls, ensuring that you and your organization adhere to the highest standards of compliance.
6. Expert Guidance: Our workshop is led by seasoned professionals with a wealth of experience in the field of HIPAA compliance. You’ll benefit from their insights and real-world examples, gaining a practical understanding of how to address HIPAA concerns in clinical trials and treatment settings.
7. Prepare for Auditing and Security: Is your organization HIPAA compliant? Learn about the factors that auditors look for when assessing compliance and proactively address potential vulnerabilities. Additionally, we’ll cover essential aspects of HIPAA Security, equipping you to safeguard patient information effectively.
By joining our HIPAA Training and Certification Workshop, you’re not just acquiring a certificate; you’re empowering yourself with the knowledge and tools to be a steward of patient rights, contributing to ethical and responsible advancements in medical research.
- Regulatory affairs professionals
- Clinical Research Professionals
- Principal Investigators
- Site Managers and Research Coordinators
- Contract Research Organizations (CROs) Staffs
- Institutional Review Board (IRB) Members
- Drug discovery and development professionals (R&D and CMC)
- Clinical trial managers
- Project Managers and Clinical trial specialists
- Pharmaceutical and Biotech Industry Professionals involved in clinical trial planning and execution.
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.
