PPTA Presents at ESID 2012

PPTA presents at the 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID 2012) held in collaboration with the International Patient Organisation of Patients with Immunodeficiency (IPOPI) and the International Nurses Group for Immune Deficiency (INGID).

October 3-6
Florence, Italy

Presentations:

"A Decision Analysis Model for Estimating Latent Therapeutic Demand for Immunoglobulin Therapy in Primary Immune Deficiencies" - Albert Farrugia, Vice President, PPTA Global Access

"The Production of Safe Plasma Derivatives from Vein to Vein" - Jan M. Bult, PPTA President and CEO

Created on June 25 2012.

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PPTA News

Final Summary of the PPTA/FDA Liaison Meeting on September 14, 2022 +

The following is a final summary of the PPTA-FDA Liaison Meeting held virtually on September 14, 2022.

Welcome, Introductions & Meeting Guidelines

PPTA and Head of Global Plasma welcomed all participants and appreciated FDA’s participation in today’s meeting. PPTA’s Head of Global Regulatory Policy opened the meeting with introductory remarks. PPTA’s External Legal Counsel advised the participants on the meeting guidelines and the antitrust statement.
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International Plasma Awareness Week 2022: Donate Locally. Think Globally. +

ANNAPOLIS, MD (October 3, 2022) — The Plasma Protein Therapeutics Association (PPTA) is proud to mark the launch of the 10th annual International Plasma Awareness Week (IPAW), which will run from Monday, October 3 until Friday, October 7. Hundreds of thousands of people in the U.S. who live with these rare diseases, and countless others facing trauma and emergency medical needs every day, rely on plasma-derived therapies that are only available because of the commitment of dedicated plasma donors.
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HHS Launches Plasma and Blood Donation Campaign +

On August 4, the U.S. Department of Health and Human Services (HHS) launched a new nationwide campaign, Giving=Living, intended to draw awareness to the importance of plasma and blood donation, especially following a steep decline in both caused by the Covid pandemic.
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PPTA Statement on the draft EU Substances of Human Origin Regulation +

PPTA welcomes positive developments but regrets missed opportunities to support plasma donors and patients who rely on plasma-derived medicinal products (PDMPs)

Brussels, Belgium (July 14, 2022). While the text of the draft regulation on Substances of Human Origin (SoHo) addresses a number of PPTA’s concerns, it has missed the opportunity to help Member States increase plasma collection to improve the reliable availability of life-saving, plasma-derived therapies to patients with a wide range of rare and complex, chronic diseases. As much as 38% of the plasma used to produce medicines for the EU’s 300,000 rare disease patients who rely on PDMPs comes from the U.S., a reliance highlighted during the pandemic, when critical plasma donations declined significantly.
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Take a tour of a plasma donation center in Frankfurt, Germany

This interactive video takes viewers through a plasma donation center in Frankfurt, Germany. Use the arrows in the upper left corner to navigate around the center.

The Source, the international magazine of the plasma protein therapeutics industry, is published three times a year.

Learn more about the need for plasma donors, plasma donation, and how you can save and improve lives.
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The need for plasma and plasma donors is more urgent than ever before. Visit givingplasma.org to learn more and to find a donation center near you.

"How Is Your Day?" is an initiative to raise awareness of the unique nature of plasma protein therapies and the value they provide to patients. It aims to inform and educate decision makers and the general public worldwide.

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PPTA Presents at ESID 2012

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