Leverancier: Certara France SARL
2 gearchiveerde aanbestedingen
Certara France SARL is van oudsher een leverancier van onderzoek en ontwikkeling, en aanverwante adviezen, advies inzake onderzoek en ontwikkeling en advies inzake onderzoek.
Historisch gezien zijn concurrerende bieders Medizinische Universität Wien, Universiteit Utrecht, University Medical Center Utrecht, Uppsala universitet, Vaccine Monitoring Collaboration for Europe, Aetion Germany GmbH, Aetion Germany GmbH, Agencia Española de Medicamentos y Productos Sanitarios en Agencia Española de Medicamentos y Productos Sanitarios.
Recente aanbestedingen waarbij de leverancier Certara France SARL wordt genoemd
2025-02-05
Quality, safety and efficacy studies of medicines (European Medicines Agency, MED - European Medicines Agency)
EMA seeks to procure the services of research organisations to perform pre- and post-authorisation studies on the quality, safety and efficacy of human and veterinary medicines, generating complementary evidence to support regulatory decision-making. The scope of research covers both nationally and centrally authorised medicinal products, as well as non-product related topics. Studies may concern research under 7 Lots: Lot 1 translational research; Lot 2 veterinary research; Lot 3 … Bekijk de aanbesteding »
EMA seeks to procure the services of research organisations to perform pre- and post-authorisation studies on the quality, safety and efficacy of human and veterinary medicines, generating complementary evidence to support regulatory decision-making. The scope of research covers both nationally and centrally authorised medicinal products, as well as non-product related topics. Studies may concern research under 7 Lots: Lot 1 translational research; Lot 2 veterinary research; Lot 3 … Bekijk de aanbesteding »
2021-03-05
Quality, Efficacy and Safety Studies on Medicines (European Medicines Agency)
Performance of pre- and post-authorisation quality, efficacy and safety research on medicines to generate data and information to support regulatory decision-making in the human and veterinary medicines regulatory domain. Bekijk de aanbesteding »
Performance of pre- and post-authorisation quality, efficacy and safety research on medicines to generate data and information to support regulatory decision-making in the human and veterinary medicines regulatory domain. Bekijk de aanbesteding »