2023 - Wearables for eCOA: Practical Considerations for Improving Patient Data Capture
Date2023-05-15
Deadline2023-05-15
VenueWebinar, USA - United States
KeywordsPatient Data; Wearables; Wearable Device
Topics/Call fo Papers
This electronic clinical outcome assessment (eCOA) webinar will explore the latest advancements in wearable technology and their potential to improve patient data collection in clinical studies. While there may still be ongoing discussions around deployment and standardization, it is clear that newer technologies such as accelerometers and video have the ability to passively or proactively gather more patient data. These wearable devices offer significant advantages in terms of capturing comprehensive and detailed information, ultimately informing the safety and efficacy of study drugs.
In this webinar, the featured speakers will take a look at the key decision drivers for consideration in deploying wearables as a means to further gather patient data, including both technical hardware considerations and regulatory requirements.
Join this webinar to learn about the benefits and considerations of utilizing wearable devices for improving eCOA patient data capture in clinical trials.
Key Takeaways:
eCOA trends including wearables
Wearable hardware: What does the ISO-13485:2016 certification mean and are all devices certified?
Is the 510K registration required?
Considerations for implementing wearables with the current eCOA strategy
Alarms and alerts considerations for including them into current eCOA solution
In this webinar, the featured speakers will take a look at the key decision drivers for consideration in deploying wearables as a means to further gather patient data, including both technical hardware considerations and regulatory requirements.
Join this webinar to learn about the benefits and considerations of utilizing wearable devices for improving eCOA patient data capture in clinical trials.
Key Takeaways:
eCOA trends including wearables
Wearable hardware: What does the ISO-13485:2016 certification mean and are all devices certified?
Is the 510K registration required?
Considerations for implementing wearables with the current eCOA strategy
Alarms and alerts considerations for including them into current eCOA solution
Other CFPs
- Drug and Device Development Outsourcing with the Research Consulting Organization (RCO) Model
- Advances in Precision Medicine, NGS Testing & Breaking Barriers with Clinical Trials
- Global Product Management: Navigating Regulatory Pressures with Automation & Interconnected Data
- New Opportunities for Value Creation: How Biotechs Can Succeed in an Increasingly Competitive Market
- Selecting Digital Health Technologies in Decentralized Clinical Trials
Last modified: 2023-05-09 06:00:31