ON-DEMAND WEBINAR · February 26, 2020
An Innovative Approach in Collecting Protocol Deviations for Clinical Trials using EDC
- Session Overview: In this webinar we will explore using EDC as a system to capture protocol deviations in near real time and discuss the benefits of trend analysis across global sites in oncology trials.
OverviewIn this webinar we will explore using EDC as a system to capture protocol deviations in near real time and discuss the benefits of trend analysis across global sites in oncology trials.
The webinar will also provide information on current industry practices, regulatory requirements and benefits of using real time protocol deviation reporting versus traditional methods.
What You'll Learn
- Awareness impact of Protocol Deviation on regulatory submission, subject safety and trial budgets.
- Understanding of current industry practices and the challenges in reporting protocol deviations.
- Explore utilizations of EDC system and techniques of collect Protocol Deviations.
- Trend analysis and KPIs.How do you make change happen?
Who Should AttendIntermediate
Clinical Data Managers
Clinical Database Programmers
Clinical Database Administrators
Other Clinical Research Professionals
Learn techniques to optimize the process of collecting PDs using EDC platform.
Standardize the process across a disease portfolio to reduce analysis time, evaluate site performance and increase patient safety.
Meet the Speaker
Associate Director, Clinical Data Management.Loona Borgohain has 15 years of experience working in the pharmaceutical and CRO industry. Loona is passionate about developing and implementing innovative techniques in collecting and analyzing clinical research data. Her goal is to bring us closer to making lifesaving drugs available to patients faster and in a more compliant manner.
She has a deep-rooted commitment to applying her knowledge and experience, to make meaningful difference in patients’ lives and fundamentally change the way cancer and rare genetic diseases are treated. She challenges herself to think big and welcomes different perspectives and backgrounds.
Loona is currently the Associate Director at Agios, a Biopharmaceutical company focused on developing breakthrough medicines for patients with cancer and rare genetic diseases.
Earn CEUsSCDM is authorized by IACET to offer 0.2 CEUs for this program. Participants are eligible to receive CEUs upon attendance and successful completion of a web-based assessment within 30 days after the webinar. CEUs are not granted after the 30-day assessment deadline.
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