PDA New England Chapter: Dinner Meeting
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Individual Registration
Group Registration
Join the PDA New England Chapter for its first dinner meeting of 2024!
Our expert guest speakers will provide an overview of the recent Annex 1 updates, including real world examples of compliance challenges and solutions, along with an introduction to contamination control strategy (CCS) and how firms can maintain Annex 1 compliance by establishing a robust CCS.
This event will take place at the Four Points by Sheraton, 1125 Boston-Providence Turnpike, Norwood, MA 02062
This event is now sold out!
Event Location
1125 Boston-Providence Turnpike, Norwood, MA 02062 Get DirectionsContact
Chapter Inquiries
Membership Services
| Registration Type | Registration Fee |
|---|---|
| Members | $85 |
| Non-Members | $155 |
| PDA Student, Retired and Unemployed Members | $20 |
Day 1
5:30pm - 6:30pm | Reception & Networking
6:30pm - 7:00pm | Dinner
7:00pm - 9:00pm | Educational Presentations
Featured Presenters
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Hilary A. Chan, MS
Principal Scientist, Global Sterility Assurance and Microbiology, Takeda
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Hilary A. Chan, MS
Takeda
Hilary Chan is a Principal Quality Control Scientist in Global Microbiology at Takeda and is based out of Lexington, MA. In her current role, Hilary is responsible for leading various technical improvement initiatives related to microbiological issues/contamination control for Takeda’s global manufacturing operations. She is a business process owner for environmental monitoring and contamination control community of practice network lead for Takeda. She is an invited speaker at industry conferences has authored various scientific publications. Hilary has 19 years of experience in the biotech industry and holds a Bachelor’s degree in Zoology from Colorado State University and a Master’s degree in Biomedical Science from Northeastern University.
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Londa Ritchey, MS, MBA
Quality Director, PharmaLex
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Londa Ritchey, MS, MBA
PharmaLex
Londa Ritchey is currently a Quality Director with the Quality Management and Compliance group within PharmaLex. Londa has 30 years of experience in pharma/biopharma/ATMP quality assurance with emphasis on sterile drug substance and drug product operations. She has worked with large and small companies through all phases of drug development and commercial production. Londa's experience includes quality risk management, aseptic quality operations, quality systems design and implementation, contamination risk management, supplier quality management, training program design and inspection readiness. Her educational background includes degrees in Microbiology, Biostatistics, and an MBA. She has a passion for coaching and challenging current thinking in the areas of compliance and quality risk management.
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