Quick links
Categories
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.
European Commission’s proposal for an EU Regulation on standards of quality and safety for substances of human origin intended for human application (SoHO Regulation)
PPTA welcomes the EU Commission proposal on a SoHO Regulation and considers it as a great opportunity to improve patient access to life-saving, highquality plasma-derived medicinal products (PDMPs), with the health and safety of patients and plasma donors at the heart of it.
All
This is some text inside of a div block.
This is some text inside of a div block.
European Commission’s proposal for an EU Regulation on standards of quality and safety for substances of human origin intended for human application (SoHO Regulation)
PPTA welcomes the EU Commission proposal on a SoHO Regulation and considers it as a great opportunity to improve patient access to life-saving, highquality plasma-derived medicinal products (PDMPs), with the health and safety of patients and plasma donors at the heart of it.
Publications
This is some text inside of a div block.
This is some text inside of a div block.
The EU Needs More Life-Saving Plasma
Plasma provides the source for life-saving treatments
All
This is some text inside of a div block.
This is some text inside of a div block.
The EU Needs More Life-Saving Plasma
Plasma provides the source for life-saving treatments
Publications
This is some text inside of a div block.
This is some text inside of a div block.
Plasma Donation is Safe
For Plasma Donation, Donor Health is the Top Priority
All
This is some text inside of a div block.
This is some text inside of a div block.
Plasma Donation is Safe
For Plasma Donation, Donor Health is the Top Priority
Publications
This is some text inside of a div block.
This is some text inside of a div block.
EU Regulation (EC) No 726/2004]
Consolidated text: Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Union procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance)Text with EEA relevance
All
This is some text inside of a div block.
This is some text inside of a div block.
EU Regulation (EC) No 726/2004]
Consolidated text: Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Union procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance)Text with EEA relevance
EU Pharmaceutical legislation
This is some text inside of a div block.
This is some text inside of a div block.
No results found