Managing medical images in clinical trials can be complex and, if not managed properly, can lead to many quality challenges and delays.
Enabling automation throughout the process can help alleviate challenges and ensure quality along every step of the trial including image upload and submission, de-identification, and data reconciliation.
Join experts from ICON Medical Imaging and Medidata for this in-depth webinar to learn how to maximize automation on your imaging trial and discuss how automation:
- Improves the quality of your data for regulatory submission
- Creates efficiencies to accelerate your trial
- Leverages integration to reduce manual steps
Speakers:
Nicole Quinlan
Director and Head of Technical Management, ICON Medical Imaging
Nicole has over 25 years of technical and management experience in the Life Sciences industry, specializing in informatics solution delivery and regulatory compliance. She has worked with diverse technologies throughout the drug development lifecycle including regulatory content management, laboratory instrumentation and information, mobile data acquisition for manufacturing, and clinical trial electronic data capture.
Andrea Falkoff
Director, Product Management, Medidata
Andrea is responsible for the Medidata Adjudicate and Rave Imaging product roadmaps. She also works directly with customers and internal stakeholders to ensure best practices are applied across imaging and endpoint adjudication trial builds. She has more than 14 years of experience working for various imaging/endpoint adjudication core labs and a proven track record for customer satisfaction and quality delivery.
Audience
The webinar will be beneficial for pharmaceutical and biotechnology professionals working in:
- Clinical Research
- Medical Imaging
- Regulatory Submission
- Data Management