About
Join us for the second interactive webinar to learn how to leverage Embase for compliant medical device submissions:

Danielle Thomas, MS, PhD, Customer consultant Embase, PharmaPendium, QUOSA, Corporate, North America and Michelle Mohsenin, Product Manager will discuss:

How to use Embase’s Simple 4 step Process to :
• Create systematic search strategies for IVD performance evaluation studies
• Create systematic search strategies for device comparison
• How to find background information on a disease of interest to determine a new IVD opportunity.

Medical Device Regulation Review:
• Review the basics of both medical device and IVD regulations for systematic reporting

Presenters
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Michelle Mohsenin
Product Manager
Michelle Mohsenin joined Elsevier’s team in 2018 as a Drug Safety/Pharmacovigilance Subject Matter Expert. She is currently supporting Elsevier’s Embase Product to ensure that Elsevier meets our customer needs. She has over 12 years of experience in Drug Safety and Pharmacovigilance. In her previous role as a Senior Drug Safety Officer at Pfizer, she was the Literature Lead managing Pfizer’s Global Literature searching including EMA’s Medical Literature Monitoring (MLM) for ICSR reporting. She also has extensive experience with regulations to ensure inspection readiness and literature management activities. Michelle is a licensed pharmacist in the state of New Jersey in the USA.
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Danielle Thomas, MS, PhD
Customer consultant Embase, PharmaPendium, QUOSA, , Corporate, North America
Danielle has a PhD in Pharmaceutical Sciences and Molecular Biology & Biochemistry. After years of research, working in drug discovery and delivery of chemotherapeutics, Danielle joined Elsevier August of 2021. Currently, Danielle is the Customer Consultant of Life Sciences products, including Embase, PharmaPendium, and QUOSA covering North America. As a Customer Consultant, she is dedicated to assisting scientists and researchers streamline their workflows by providing customized training sessions.
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