2025 PDA Week Archive
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Call for Abstract
Submission Deadline: 3/6/2025
See What Made 2024 Unforgettable!
Past Event Recap
Plan Your Productive Week
PDA Week Schedule .
Discover What's Happening Each Day with Our PDA Week Schedule
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2025 PDA Annual Meeting
25-27 March
Palm Springs, CA
Call for Abstract
Submission deadline
03/01/2025
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Ut a nisl id ante tempus hendrerit. Vestibulum volutpat pretium libero. Aenean imperdiet. Praesent ut ligula non mi varius sagittis. Duis lobortis massa imperdiet quam. Proin magna. Phasellus blandit leo ut odio. Sed in libero ut nibh placerat accumsan. Phasellus nec sem in justo pellentesque facilisis. Nam pretium turpis et arcu.
Nulla facilisi. Proin viverra, ligula sit amet ultrices semper, ligula arcu tristique sapien, a accumsan nisi mauris ac eros. Vivamus aliquet elit ac nisl. Etiam imperdiet imperdiet orci. Phasellus nec sem in justo pellentesque facilisis. Praesent ut ligula non mi varius sagittis. In consectetuer turpis ut velit. Morbi ac felis. Cras dapibus. Aenean viverra rhoncus pede.
Discover What's Scheduled
Agenda .
Explore Our Event Agenda
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2025 PDA Annual Meeting
25-27 March
Palm Springs, CA
Call for Abstract
Submission deadline
03/01/2025
Labore saepe, aut eveniet incidunt reprehenderit. Iure vel molestiae dignissimos laboriosam quam nostrum explicabo expedita dolor tempore fuga odio odit placeat quo ipsum rerum unde ex tenetur, harum eius cupiditate libero quos! Accusamus mollitia eum, in aperiam veritatis alias eius ipsum dignissimos eligendi totam, atque impedit minima, ipsa enim.
Ut a nisl id ante tempus hendrerit. Vestibulum volutpat pretium libero. Aenean imperdiet. Praesent ut ligula non mi varius sagittis. Duis lobortis massa imperdiet quam. Proin magna. Phasellus blandit leo ut odio. Sed in libero ut nibh placerat accumsan. Phasellus nec sem in justo pellentesque facilisis. Nam pretium turpis et arcu.
Nulla facilisi. Proin viverra, ligula sit amet ultrices semper, ligula arcu tristique sapien, a accumsan nisi mauris ac eros. Vivamus aliquet elit ac nisl. Etiam imperdiet imperdiet orci. Phasellus nec sem in justo pellentesque facilisis. Praesent ut ligula non mi varius sagittis. In consectetuer turpis ut velit. Morbi ac felis. Cras dapibus. Aenean viverra rhoncus pede.
Plan Your Journey
Travel .
Travel Details and Accommodations
Conference Venue
The Palm Springs Hotel, Palm Springs
2135 N Palm Canyon Dr
Palm Springs, CA 92262
Hotel Accommodations
Hyatt Regency Lisbon
Rua da Junqueira, 65, 1300-343
Lisbon, Portugal
Hotel: +351 21 241 1234
Room Rate: View the website for rates.
Check-in: 1500
Check out: 1200
There are many hotel options near the Lisbon Congress Center, which is the venue of the 2024 PDA Europe Annual Conference. Below are two options identified near the congress center. Please click on the "Book a Room" buttons to view rates and book directly with the hotel. Credit card details will be requested to confirm your reservation. View the full list of additional hotels.
Hyatt Regency Lisbon
Rua da Junqueira, 65, 1300-343
Lisbon, Portugal
Hotel: +351 21 241 1234
Room Rate: View the website for rates.
Check-in: 1500
Check out: 1200
Hyatt Regency Lisbon
Rua da Junqueira, 65, 1300-343
Lisbon, Portugal
Hotel: +351 21 241 1234
Room Rate: View the website for rates.
Check-in: 1500
Check out: 1200
Meet our Expert Presenters
Presenters .
Learn from Industry Leaders
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Maggie Reiff-Bandel MBA
Read Bio
Maggie Reiff-Bandel MBA
Maggie Bandel has 10 years industry experience covering diagnostics, class I and II medical devices, pre-filled syringes, pen injectors, autoinjectors, novel drug delivery systems, and advanced therapies. Her experience spans all product life stages, from early-stage R&D through lifecycle management, covering a wide range of pharmaceutical products through her various leadership roles. Maggie currently leads the PDA Combination Products Steering Committee, providing input and oversight into critical areas within the industry. After spending the last few years leading various start-up R&D organizations, Maggie now consults for Johnson and Johnson. Maggie holds an MBA from Rutgers University and a B.S in Biomedical Engineering from UNC/NC State University. -
Maria Amaya PhD
Genentech
Maria Amaya, PhD, is the Lead External Advocacy, North America in Quality Policy & Advocacy at Roche. In this position, Maria works within the Roche/Genentech Global External Advocacy community to develop and deliver innovative quality and current GMP regulatory pathways and collaborate with internal and external stakeholders, including support in harmonization and streamlining of regulations. Maria has more than 15 years of experience in the pharmaceutical industry working in product development, manufacturing technology, regulatory, and quality, and compliance. Maria holds a PhD in protein chemistry, a Master of Science in protein engineering from the Paris-Sud University in France, and a Bachelor of Science in chemistry from the National University in Colombia. -
Alexander Aust
Aust Business Solutions
Alexander Aust, MS, MBA is a nonviral drug delivery system (DDS) expert, strategic operations leader, and biopharma industry investor. Alexander is the CEO of Aust Business Solutions (AUST), a consulting firm that has distinguished itself in the areas of Cell and Gene Therapeutics (CGT), Aseptic Processing, and GMP Quality Support. AUST accomplishes a variety of Technical activities and functions as a Virtual CDMO; these projects often include facility design, technology transfers, process development, supply chain management, project management, regulatory submission authoring, FDA communication, CMC support, auditing, business operations, marketing, and market analysis. Alexander studied Molecular and Cellular Biology at Purdue University as well as Manufacturing and Operations Management at Ball State University. He has spent the last 12 years working with Biologics at all stages of life cycle development and commercialization. Alexander has been particularly successful with the development, manufacture, and testing of lipid and polymer-based DDS in support of targeted drug delivery. Starting with PEGylated proteins, liposomal formulations, peptides, CRISPR, and mRNA, Alexander has influenced innovation and driven growth in the space of lipid nanoparticle (LNP) functionality before, during, and after the COVID pandemic. He hopes to share his insights regarding advances in nanoparticle delivery vehicle development with you. -
Hal Baseman MBA
ValSource, Inc.
Hal Baseman is Vice President at ValSource Inc. He has over 45 years of experience in pharmaceutical operations, validation, and regulatory compliance. He has previously held positions as the Chair of the PDA (Parenteral Drug Association) Board of Directors, the Co-Chair of the PDA Science Advisory Board, the Co-Leader of the PDA Aseptic Processing Points to Consider Task Force and the Co-Leader of the PDA Process Validation Interest Group. He is currently the Co-Chair of the PDA Annex 1 Response Team, as well as a long-time member of the PDA Training Research Institute faculty. Hal holds an MBA in Management from LaSalle University and a B.S. in Biology from Ursinus College. -
Arie Anahory Masters of Science
Regulatory Compliance Associates Inc.
Serving as Senior Director, Strategy and Customer Excellence for Regulatory Compliance Associates@ inc., Arielle Anahory provides guidance to life-science clients experiencing operational challenges in the compliance, regulatory, quality assurance, R&D, and operational processes of the product lifecycle. Arielle Anahory oversees large and complex projects from procurement through contract closeout, which includes supervising the development of budgets and schedules, managing employee performance, reporting progress, and initiating action to assure program objectives and schedules are met and work is performed within budget and according to the specification of life-science processes. Most importantly, Arielle provides key communication amongst project teams and senior management. -
Denyse Baker PE, RAC
Eli Lilly and Company
Denyse Baker is the Associate Vice President, External Engagement and Advocacy, for the Global Quality Compliance organization at Eli Lilly. She is passionate about connecting and collaborating to develop science-based regulation and organizational quality culture as to enable production of high quality products for patients. Denyse has a strong technical foundation to her policy work with experience in engineering, manufacturing, quality and regulatory for small molecules, biologics and devices. Denyse returned to Lilly in December 2022 following work experience with the US FDA, the Parenteral Drug Association, and AstraZeneca. She is a member of the Global Quality Management WG at PhRMA, Vice-Chair of PDA’s Regulatory and Quality Advisory Board, Co-leader of the PDA Quality Management Maturity Task Force, and secretary to the FDA Alumni Association Board of Directors. Denyse holds a B.S. in Mechanical Engineering from Northwestern University, is a licensed professional engineer, and earned RAC certifications in US and EU Reg Affairs. -
Janmeet Anant PhD
MilliporeSigma
Janmeet Anant, Ph.D., PMP, RAC serves as a Senior Regulatory Consultant at MilliporeSigma, focused on pharmaceutical manufacturing, specifically working on sterile injectables. Janmeet has served as an Executive Board Member for the Bioprocess Systems Alliance (BPSA), Vice-Chair of a subcommittee of the American Society of Mechanical Engineers - Bioprocessing Equipment (ASME-BPE) standard setting organization, and a member of the Regulatory Governance Team at BioPhorum. With over 20 years of experience in the pharmaceutical industry, Janmeet has been consulting on complex regulatory strategy projects with pharmaceutical drug manufacturers, leveraging skills from his Project Management Professional (PMP) and Regulatory Affairs Certification (RAC). Janmeet has a Bachelor of Science degree in Chemistry and a Ph.D. in Pharmacology. -
Jason Angstadt MS
Lyophilization Technology Inc.
Jason B. Angstadt is a Scientist III at Lyophilization Technology Inc. He has spent 10 years in the field of lyophilization and sterile products. He started his career in lyophilization as a technician in the lab and proceeded to advance the the Scientist and Project Director role where he has spent the last 5 years of his career. As a Project Director and Scientist, Jason is responsible for project coordination from concept through technical support, troubleshooting, and clinical trial material manufacturing. The first few years of his career were in medical device. Jason earned his Bachelor of Sceince degree from Albright College co-majoring in Biology and History. He also holds a Masters in Pharmaceutical Science from Temple University. In his free time, Jason likes to spend time with his wife and daughter, golf, run, read, and play with his two dogs.
