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EU Pharmaceutical legislation

EU PHARMACEUTICAL LEGISLATION

In order to ensure regular access to plasma medicines for those in need, it is critical that policymakers acknowledge the clinical urgency for increased plasma collection in Europe. Discover the latest updates on legislation surrounding the broader European plasma donation ecosystem.

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3d shape in blue, customized according to PPTA's branding

3d shape in blue, customized according to PPTA's branding

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PPTA position paper on the importance of the EU-US MRA for patient access to plasma-derived medicinal products (PDMPs)

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PPTA position paper on the importance of the EU-US MRA for patient access to plasma-derived medicinal products (PDMPs)

EU pharmaceutical legislation

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PPTA position paper on the revision of the general EU pharmaceutical legislation - English

PPTA position paper on the evaluation of the EU pharmaceutical legislation

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PPTA position paper on the revision of the general EU pharmaceutical legislation - English

PPTA position paper on the evaluation of the EU pharmaceutical legislation

EU pharmaceutical legislation

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European Commission: Roadmap

The EU is launching a new strategy to improve and accelerate patients’ access to safe and affordable medicines and to support innovation in the EU pharmaceutical industry.

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European Commission: Roadmap

The EU is launching a new strategy to improve and accelerate patients’ access to safe and affordable medicines and to support innovation in the EU pharmaceutical industry.

EU pharmaceutical legislation

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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

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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

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