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Dec 21, 2023
The Source: Winter 2023
In this issue: Maintaining Donor Health and Safety: Review of Recently Published PPTA Donor Health Studies; Learn More About the 2023 Joachim Hilfenhaus Award Recipient, Thomas R. Kreil, Ph.D., Takeda; European Plasma Alliance Unveils Revamped Website and Logo; PPTA Members and Patient Groups Join to Advocate on Capitol Hill; Getting to Know the New Chair of the North America Board of Directors — Adam Grossman, ADMA Biologics, and more.
All
The Source Magazine
https://bit.ly/3vQ4r9i
Dec 21, 2023
The Source: Winter 2023
In this issue: Maintaining Donor Health and Safety: Review of Recently Published PPTA Donor Health Studies; Learn More About the 2023 Joachim Hilfenhaus Award Recipient, Thomas R. Kreil, Ph.D., Takeda; European Plasma Alliance Unveils Revamped Website and Logo; PPTA Members and Patient Groups Join to Advocate on Capitol Hill; Getting to Know the New Chair of the North America Board of Directors — Adam Grossman, ADMA Biologics, and more.
All
The Source Magazine
https://bit.ly/3vQ4r9i
Dec 18, 2023
PPTA Statement on Issuance of the EU Critical Medicines List
All
PPTA statements
Dec 18, 2023
PPTA Statement on Issuance of the EU Critical Medicines List
All
PPTA statements
Dec 1, 2023
PPTA Statement and Reflection on the Quebec Biovigilance Committee’s 8th Biovigilance Forum
All
PPTA statements
Dec 1, 2023
PPTA Statement and Reflection on the Quebec Biovigilance Committee’s 8th Biovigilance Forum
All
PPTA statements
Nov 8, 2023
Summary of the PPTA/FDA Liaison Meeting (November 8, 2023)
PDMPs — which are derived from human plasma from healthy donors — are essential for around 300,000 European patients who rely on these therapies to treat a variety of rare, chronic, and potentially life-threatening conditions, which are often genetic in origin. Without these treatments, many patients might not survive or would have a substantially diminished quality of life. In addition, plasma-derived medicines are also used in everyday treatment, such as supportive treatment in trauma cases, liver disease, cardiac surgery, and in some cases, pregnancy complications.
All
PPTA statements
https://cdn.prod.website-files.com/638f893112c6eac0e46ac576/657b49c161b36be580c14e84_2023%20FDA%20Liaison%20Meeting%20Summary_Website_FINAL.pdf
Nov 8, 2023
Summary of the PPTA/FDA Liaison Meeting (November 8, 2023)
PDMPs — which are derived from human plasma from healthy donors — are essential for around 300,000 European patients who rely on these therapies to treat a variety of rare, chronic, and potentially life-threatening conditions, which are often genetic in origin. Without these treatments, many patients might not survive or would have a substantially diminished quality of life. In addition, plasma-derived medicines are also used in everyday treatment, such as supportive treatment in trauma cases, liver disease, cardiac surgery, and in some cases, pregnancy complications.
All
PPTA statements
https://cdn.prod.website-files.com/638f893112c6eac0e46ac576/657b49c161b36be580c14e84_2023%20FDA%20Liaison%20Meeting%20Summary_Website_FINAL.pdf
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