The webinar has been recorded and is available for free. Please select the links for access.
This webinar will cover several aspects of the conference including:
- The format of the conference and an overview of the schedule
- Educational Program
- Conference session highlights
- Workshop details
- Keynote speaker highlights
- Roundtable Discussion overview
- Why you should attend Excipient World
- How to navigate the website (a comprehensive review will be performed)
- How to register for the event
- Vendor/Exhibitor overview
- Details about the location and venue
The webinar is a free, 30 minute presentation & 30 minute question and answer session about Excipient World 2019.
Bretta Lichtenhan is Head of Pharma Registrations within Pharma Food Materials organization of the Life Science division of MilliporeSigma. She manages a global team of regulatory experts, focused on regulatory registration of products such as active pharmaceutical ingredients (APIs), highly potent APIs, linkers, antibody-drug conjugates, excipients, and pharmaceutical materials for the (bio-) pharmaceutical industry. Bretta also currently serves as Chair-Elect of IPEC-Americas, an industry association focused on advocating, educating, innovating and developing best practices for excipients, with a focus on patient safety. She has over 22 years of experience in the industry with previous experience at Biopharma companies Genzyme (a Sanofi Company) and Percivia LLC. Bretta has worked for MilliporeSigma for over 10 years in various roles from R&D Product Development, Product Management, Business Development and Regulatory Affairs. Bretta has a bachelor’s degree in Biology from the University of New Hampshire and Master’s of Biotechnology Engineering from Tufts University in the United States.
Heather’s current role is Sr. Manager, Raw Materials Strategy within the Global Technical Operations department of the Johnson & Johnson Family of Consumer Companies focusing on technical aspects of raw materials and raw material qualification. She currently leads a global team and manages the raw material portfolio within the Self Care sector of Johnson and Johnson. She has worked in the Pharmaceutical Industry for 15+ years in Process Development, Technical Transfer and Raw Material Evaluation roles. She currently Vice Chairs the IPEC Americas Excipient Qualification Committee, is the Vice Chair of User Relations, and is heavily involved in the education committee for IPEC’s ExcipientWorld.