SAVE THE DATE!
IPPC 2026 will be held 21-22 April in Milan, Italy.
ABOUT THE CONGRESS
At the heart of our congress is a commitment to the entire value chain of PDMPs – from vein to vein, from donor to patient. Through insightful sessions, engaging discussions, and networking opportunities, participants will learn about European strategies for strengthening medical supply chains, global perspectives on improving patient access, and the essential role of dedicated healthy donors.
IPPC 2025 PROGRAM
Day One - Tuesday, 20 May 2025
TIME (GMT+1)
07:30 - 17:30
On-site registration open
09:00 - 09:15
Welcome & Opening Ceremony
Anita Brikman, President and CEO - PPTA
Video Message
Adam Jarubas, Ph.D., Member of the European Parliament, Chair of the Committee on Public Health (SANT)
09:15 - 10:00
Plenary Session: Trade & Tariffs: Trump 2.0 and Its Effect on the Plasma Industry: A Discussion of Key Issues
Paul Rosenthal, a leading Washington D.C.-based international trade lawyer, joins PPTA’s VP of Government Affairs, Sharon Pearce, and Senior Director, Global Plasma & International Affairs, Julia Fabens, to provide an overview of the first 100 days of the Trump Administration, and how its moves on tariffs, trade, border security, regulatory authority, and other policy issues may impact Europe and the PDMP industry.
Speakers:
Paul Rosenthal, Trade Expert - Kelley Drye & Warren LLP
Sharon Pearce, Vice President, Government Affairs - PPTA
Julia Fabens, Senior Director, Global Plasma and International Affairs - PPTA
10:00 - 10:45
SESSION 1: Patient-Driven Progress: Advancing Plasma-Derived Medicines & Addressing Disparities
Patients and patient advocates discuss the last two decades of progress in disease diagnosis, patient access to plasma-derived medicinal products (PDMPs), policy, and more. Kick off IPPC with a look at the past, present, and future of patient need.
Moderator: Sarah-Taïssir Bencharif, M.D., Freelance Health Journalist, Event Moderator, and Emergency Physician
Speakers:
Matine Pergent, President - International Patient Organisation for Primary Immunodeficiencies (IPOPI)
(VIRTUAL) Fernanda Aspilche Ferro, President - Alpha-1 Europe
Nancy Di Salvo, International Affairs Director - GBS/CIDP Foundation International
Nathan Schaefer, Public Policy - World Federation of Hemophilia
10:45 - 11:30
Networking Break
11:30 - 12:45
SESSION 2: Critical Medicines: European Strategies for Preventing Shortages and Securing Supply
Dive into the European Union’s latest efforts to strengthen medical supply chains, prevent disruptions, and improve the resilience of health care systems during emergencies. Experts will unpack key initiatives such as the Pharmaceutical Legislation, the Critical Medicines Act, and the European Shortages Monitoring Platform (ESMP). Find out what is new and changing in this area and why it matters for plasma-derived medicines.
Moderator: Vasiliki Angouridi, Health Editor - Euractiv
Speakers:
Sandra Dang, Medicines and Medical Devices Shortages Officer - European Medicines Agency
Steffen Mager, Vice President of Biopharma Sales & Commercial Operations Europe - Grifols
Leire Solis, Director for Health Policy and Advocacy - International Patient Organisation for Primary Immunodeficiencies (IPOPI)
(VIRTUAL) Stefaan Van der Spiegel, Head of Sector - Substances of Human Origin (SoHO - blood, tissues, cells, organs) - European Commission
12:45 - 14:00
Networking Lunch
14:00 - 15:15
SESSION 3: Pushing Barriers: Global Perspectives on Improving Patient Access
Examine the global landscape of patient access to plasma-derived medicines. Understand the challenges that limit access for patients outside of Europe and the U.S., and discover the innovative solutions being used in diverse regions of the world.
Moderator: Svenja Barckhausen, CEO and Founder - Blood Plasma Strategy Experts UG
Speakers:
Dana Miloslavich, Director of Research - Marketing Research Bureau
Juçaíra Stella M Giusti, Associação Eu Luto Pela Imuno Brasil- ELPIB
Nariman Sadri, CEO - Darman Ara Co.
Tineke Zurrbier, Public Affairs and Advocacy Lead, Plasma Derived Therapies - Takeda
Dr. Amin Magdy, CEO - Grifols Egypt
15:15 - 16:00
Networking Break
16:00 - 17:15
SESSION 4: Innovation: What’s Next for PDMPs?
Discover the latest innovations in research and development of plasma-derived medicines. Attendees will learn about the industry’s ongoing work to develop novel therapies, and explore new, evidence-based indications for already approved therapies.
Moderator: John Curling, Independent Consultant - JCC AB
Speakers:
Joerg Schuettrumpf, Chief Scientific Innovation Officer - Grifols
Rudolf Hartmann, Head of PDT Analytical Development - Takeda
Andrea Denardo, Specialist, Research and Innovation - Kedrion
17:15 - 17:30
End of the Day Closure and Presentation of the Hilfenhaus Award
Presented by: Ferdinando Borgese, Vice President Intercontinental Region & ICM - Kedrion Biopharma and Chair of PPTA Europe
17:30 - 19:30
Networking Reception in the Exhibit Hall/Foyer - Sponsored by ImmunoTek Bio Centers
Day Two - Wednesday, 21 May 2025
TIME (GMT+2)
08:00 - 15:00
On-site registration open
08:30 - 08:45
Day Two Kickoff and Welcome
08:45 - 09:30
Leadership Perspectives: Navigating an Evolving Industry & World
Join PPTA President and CEO Anita Brikman for an intimate conversation with industry leaders. Senior executives from Grifols, Kedrion, and Takeda will share lessons learned on leadership, growth, resilience, and innovation.
Moderator: Anita Brikman, President & CEO - PPTA
Speakers:
Ugo Di Francesco, Chief Executive Officer - Kedrion
David Bell, Chief Corporate Affairs and Legal Officer - Grifols
Margaret Drysdale, PDT Regional Commercial Strategy Head - Takeda
09:30 - 10:45
SESSION 5: Methodologies in Donor Health and Safety Research
Learn about how ongoing research is contributing to future improvements in plasma donor safety. This session will offer an overview of using real world data to produce real world evidence in research surrounding global donor health and safety.
Moderator: Lise Estcourt, M.D., Medical Director for Transfusion - NHS Blood and Transplant (NHSBT); Medical Director of NHSBT Clinical Trials Unit - NHSBT
Speakers:
(VIRTUAL) Juan Jose Abellan-Andres, Ph.D., Biostatistics and RWE Senior Specialist, Data Analytics and Methods Task Force - European Medicines Agency
Eva Hellman, Director Clinical Affairs - Haemonetics
Michelle Fransen, MPH, Director, Study Management - PPTA
10:45 - 11:00
Special Segment: "It's my Movie Time" - Hear from a Plasma Donor
Pauline Meßner, a plasma donor in Germany, takes the stage with Britta Diebel of Haema to share what inspired her to donate in the first place, why she finds donation meaningful, and how she shares plasma donation with her community. Plus, as a fan of visual media, Pauline will share her latest film & TV recommendations, as watching a show or a movie while donating is her favorite way to pass the time!
Speakers:
Pauline Meßner - Plasma donor
Britta Diebel, Manager Communications Plasma Europe - Haema GmbH
11:00 - 11:30
Networking Break
11:30 - 12:45
SESSION 6: Building a Resilient Supply of Plasma for Fractionation
Hear lessons learned around building a resilient global plasma supply chain that meets growing patient demand. Experts will address key issues such as the value of public-private coexistence and leveraging the implementation of the Substances of Human Origin (SoHO) legislation. This discussion includes a variety of innovative practices that model a sustainable and resilient supply chain.
Moderator: Brad Pick, Senior Director Global External Communications - Grifols
Speakers:
(VIRTUAL) Stefaan Van der Spiegel, Head of Sector - Substances of Human Origin (SoHO - blood, tissues, cells, organs) - European Commission
Milan Maly, Chairman - European Plasma Alliance
Jean-Philippe Plançon, President - EPODIN
Mag. Dr. Karmin Saadat, Department Good Manufacturing Practice - Austrian Agency for Health and Food Safety (AGES)
Lorenzo Montrasio, Advisor to the Italian Blood Centre & the Italian Presidency of Ministers for Health Literacy
12:45 - 14:00
Networking Lunch
14:00 - 15:15
SESSION 7: Ensuring Access: The Role of Market Policies for PDMPs - Role of National Medicines Policies
Explore market access policies surrounding plasma-derived medicines, such as mandatory stockpiling and restrictive reimbursement policies. Understand the impact of economic measures on plasma-derived medicines and the patients they benefit from. The session offers policy recommendations and discusses the necessity of shifting from “one-size-fits-all” policies to more patient-centric, tailored approaches.
Moderator: Tomasz Kluszczyński, Director - ACESO Healthcare Consulting
Speakers:
Dr. Tobias Volkwein, Partner - D+B Lawyers
Jakub Dvořáček, Deputy Minister for Health Czech Republic
Adrian Goretzki - Healthcare Education Institute (EDU) & Patient Advocate
Anna Kostera-Pruszczyk, Professor of Neurology & Pediatric Neurologist - Medical University of Warsaw
Natalia Bartosik, Global Value & Access Lead - Takeda
15:15 - 15:30
Closure of IPPC 2025
*Subject to change
Why attend
- Insightful discussions: Gain valuable insights from thought-provoking sessions featuring expert panelists.
- Advocacy opportunities: Join the conversation on shaping policies and initiatives that promote access, safety, and sustainability in PDMPs.
- Networking: Connect with industry leaders, policymakers, health care professionals, and patient advocates from around the globe.
- Interactive showcase: Discover innovative products, services, and technologies from leading industry suppliers and partners.
WHO SHOULD ATTEND
The International Plasma Protein Congress invites professionals and stakeholders from across the plasma protein industry, including:
- Donor organizations
- Health care providers
- Regulatory agencies
- Industry suppliers
- Patient advocacy groups
CONTACTS
Hotel and Congress inquires
Melanie Conrads
MConrads@pptaglobal.org
+32.2.724.0188
Registration inquires
Charon Smith
csmith@pptaglobal.org
+1.410.432.4921
Sponsorship and Exhibit inquires
Michelle Mason
mmason@pptaglobal.org
+1.443.370.6056