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Actors and Networks database

The evolving field of gene and cell therapy is supported by a large community of academic, clinical, translational, regulatory and patient organisations. The Actors and Networks database maps these stakeholders in Europe and beyond, their activities, and resources they have produced. 

EuroGCT has developed and compiled this database for those interested in identifying the actors involved at each stage of the pathways bringing gene and cell therapies from lab to clinic. Coming from an academic perspective, our focus is to map information that has not been mapped elsewhere. This includes documenting the various types of interconnected regulators, patient groups actively involved along the pathways, and non-profit organisations devoted to therapy development. In its first iteration, this database does not yet include commercial partners and service providers.

Additional complementary work by other organisations on GCT stakeholders mapping can be found here.

A scientific paper on actors has also been published in Humanities and Social Sciences Communications. You can find its lay summary here.

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Czech Office for Standards, Metrology and Testing (Úřad pro technickou normalizaci, metrologii a státní zkušebnictví) (ÚNMZ)

Region/Country:  
  • Countries in the EU/EEA
  • Czechia

Type of Actor:

  • Regulators
  • Medical Devices Entities
  • Medical Device Authorities
  • National Medical Device Authorities

Development Stage:

  • Manufacturing
  • Commercialisation

Czech State Institute for Drug Control (Státní ústav pro kontrolu léčiv) (SÚKL)

Region/Country:  
  • Countries in the EU/EEA
  • Czechia

Type of Actor:

  • Regulators
  • HTA Bodies
  • Medicines Agencies
  • National Medicines Agencies
  • Medical Devices Entities
  • Medical Device Authorities
  • National Medical Device Authorities
  • Other National competent authorities
  • Competent Authorities for Tissues and Cells
  • Competent Authorities for Blood and Blood Components
  • Competent Authorities for GMO

Development Stage:

  • Fundamental Research
  • Clinical Research
  • Manufacturing
  • Commercialisation

Additional information

The Czechia State Institute for Drug Control is a Czech government agency responsible for regulation of the safe production of pharmaceuticals in the country, clinical evaluation of medicines and for monitoring the advertising and marketing of both medicines and medical devices.

Danish Data Protection Agency (Datatilsynet)

Region/Country:  
  • Countries in the EU/EEA
  • Denmark

Type of Actor:

  • Regulators
  • Data Authorities
  • National Data Authorities

Development Stage:

  • Fundamental Research
  • Clinical Research
  • Translational Research
  • Health Data

Danish Environmental Protection Agency (Miljøstyrelsen)

Region/Country:  
  • Countries in the EU/EEA
  • Denmark
Website:  

Type of Actor:

  • Regulators
  • Other National competent authorities
  • Competent Authorities for GMO

Development Stage:

  • Fundamental Research
  • Clinical Research
  • Manufacturing
  • Commercialisation

Danish Health Technology Council (Behandlingsrådet)

Region/Country:  
  • Countries in the EU/EEA
  • Denmark

Type of Actor:

  • Regulators
  • HTA Bodies

Development Stage:

  • Commercialisation

Danish Medicines Agency (Lægemiddelstyrelsen) (DKMA)

Region/Country:  
  • Countries in the EU/EEA
  • Denmark

Type of Actor:

  • Regulators
  • Medicines Agencies
  • National Medicines Agencies
  • Medical Devices Entities
  • Medical Device Authorities
  • National Medical Device Authorities
  • HTA Bodies
  • Medical Devices Entities
  • Medical Device Authorities
  • National Medical Device Authorities
  • Competent Authorities for GMO

Development Stage:

  • Fundamental Research
  • Clinical Research
  • Manufacturing
  • Commercialisation

Additional information

The Danish Medicines Agency authorises and inspects pharmaceutical companies and licenses medicinal products in the Danish market.

Danish Medicines Council (Medicinrådet)

Region/Country:  
  • Countries in the EU/EEA
  • Denmark

Type of Actor:

  • Regulators
  • HTA Bodies

Development Stage:

  • Commercialisation

Danish National Committee on Health Research Ethics (Nationale Videnskabsetiske Komité) (NVK)

Region/Country:  
  • Countries in the EU/EEA
  • Denmark

Type of Actor:

  • Regulators
  • Other National competent authorities
  • Competent Authorities for GMO

Development Stage:

  • Fundamental Research
  • Clinical Research
  • Manufacturing
  • Commercialisation

Danish Patient Safety Authority (Styrelsen for Patientsikkerhed) (STPS)

Region/Country:  
  • Countries in the EU/EEA
  • Denmark
Website:  

Type of Actor:

  • Regulators
  • Other National competent authorities
  • Competent Authorities for Tissues and Cells
  • Competent Authorities for Blood and Blood Components

Development Stage:

  • Manufacturing
  • Commercialisation

Additional information

The Danish Patient Safety Authority is the competent authority for tissues and cells and for blood and blood components in Denmark.

Danish Working Environment Authority (Arbejdstilsynet)

Region/Country:  
  • Countries in the EU/EEA
  • Denmark
Website:  

Type of Actor:

  • Regulators
  • Other National competent authorities
  • Competent Authorities for GMO

Development Stage:

  • Fundamental Research
  • Clinical Research
  • Manufacturing
  • Commercialisation
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