Genes, cells, and tissues based medicinal products are specifically regulated as Advanced Therapy Medicinal Products (ATMPs) within the European Union (EU) from the adoption of Regulation (EC) n°1394/2007 on ATMPs. Beyond legislative requirements, the complexity and scientific technicity of these medicines, as well as the necessary flexibility to take into account the evolutions and the scientific and regulatory experience gained has led to the development of an important amount of guidelines in the field.These guidelines have mainly been adopted by the European Medicines Agency (EMA), the European regulatory agency especially in charge of the scientific assessment of medicines to be commercialized in the EU. Some of them have also been ado...
International audienceIn the European Union, gene and cell therapy medicinal products are mainly reg...
A comparative analysis of assessment procedures for authorization of all European Union (EU) applica...
In the EU, a medicinal product needs a marketing authorization (MA) to be placed on the market. The ...
In an effort to help stakeholders to overcome the legal and scientific challenges raised during the ...
International audienceAdvanced Therapy Medicinal Products (ATMPs), a European legal classification o...
Many actors influence the framing of EU legislation and regulation applicable to gene and cell thera...
Advanced therapy medicinal products (ATMPs) are a fast-growing field of innovative therapies. The Eu...
Advanced Therapy Medicinal Products (ATMPs) is a European classification of medicinal products based...
Advanced Therapy Medicinal Products (ATMPs) is a European classification of medicinal products based...
Even for centrally approved products, each European country is responsible for the effective nationa...
Recent advances in biomedicine are opening the door to new approaches, and treatment and prevention ...
In 2007, the European Union adopted a lex specialis, Regulation (EC) No. 1394/2007 on advanced thera...
Advanced therapy medicinal products (ATMPs) such as gene-, cell- and tissue engineered therapies off...
Advanced therapy medicinal products (ATMPs) have a massive potential to address existing unmet medic...
Advanced Therapy Medicinal Products (ATMPs) comprising cell, gene, and tissue-engineered therapies h...
International audienceIn the European Union, gene and cell therapy medicinal products are mainly reg...
A comparative analysis of assessment procedures for authorization of all European Union (EU) applica...
In the EU, a medicinal product needs a marketing authorization (MA) to be placed on the market. The ...
In an effort to help stakeholders to overcome the legal and scientific challenges raised during the ...
International audienceAdvanced Therapy Medicinal Products (ATMPs), a European legal classification o...
Many actors influence the framing of EU legislation and regulation applicable to gene and cell thera...
Advanced therapy medicinal products (ATMPs) are a fast-growing field of innovative therapies. The Eu...
Advanced Therapy Medicinal Products (ATMPs) is a European classification of medicinal products based...
Advanced Therapy Medicinal Products (ATMPs) is a European classification of medicinal products based...
Even for centrally approved products, each European country is responsible for the effective nationa...
Recent advances in biomedicine are opening the door to new approaches, and treatment and prevention ...
In 2007, the European Union adopted a lex specialis, Regulation (EC) No. 1394/2007 on advanced thera...
Advanced therapy medicinal products (ATMPs) such as gene-, cell- and tissue engineered therapies off...
Advanced therapy medicinal products (ATMPs) have a massive potential to address existing unmet medic...
Advanced Therapy Medicinal Products (ATMPs) comprising cell, gene, and tissue-engineered therapies h...
International audienceIn the European Union, gene and cell therapy medicinal products are mainly reg...
A comparative analysis of assessment procedures for authorization of all European Union (EU) applica...
In the EU, a medicinal product needs a marketing authorization (MA) to be placed on the market. The ...