The success of mRNA-based vaccines for COVID-19 lays the path to accelerate the development of this modality for many other diseases. Key decisions must be made early in the drug development process for all aspects: from mRNA manufacturing to sourcing of critical components such as lipid excipients for the final formulation. Doing a deep dive into the critical aspects of these lipids, this webinar aims to highlight that considerations such as excipient quality can significantly impact the performance, reproducibility, costs, and regulatory timelines of the final drug product.
In this webinar, you will discover:
- How we got to the lipid nanoparticles we have today
- Key considerations for their formulation
- What's important to keep in mind when choosing lipid excipients for the development of your drug product
Speaker
Estelle Beguin, Ph.D.
Merck
Strategic Marketing Manager - Synthetic Lipids
Estelle has experience working as a formulation and process engineer on drug delivery programs for several biotech companies in Boston. She has joined Merck as a global strategic marketing manager for synthetic lipids. In this role, she is responsible for managing the lipids portfolio and custom manufacturing businesses supporting top industry players and young start-ups in the fields of RNA delivery and vaccines. She holds a Ph.D. in Engineering Science from the University of Oxford, the U.K. where she worked on developing ultrasound-responsive lipid-based drug delivery systems.
Pharma and biopharma manufacturing
- Solid Formulation Strategies
기간:1h
언어:English
세션 1:발표 완료 July 21, 2022
계속 읽으시려면 로그인하거나 계정을 생성하세요.
계정이 없으십니까?