Health technology assessments for medicines should be broader, says an international report commissioned by R&D-based pharmaceutical industry associations from Europe, the US and Australia 1 ,2 . Assessments that take on the views of wider ...
Belén Crespo Sánchez-Eznarriaga has been appointed director of the Spanish healthcare products regulatory agency, the AEMPS (Agencia Española de Medicamentos y Productos Sanitarios) 1 . Ms Crespo replaces Cristina Avendaño, who had held the post ...
Belén Crespo Sánchez-Eznarriaga has been appointed director of the Spanish healthcare products regulatory agency AEMPS (Agencia Española de Medicamentos y Productos Sanitarios) 1 . She replaces Cristina Avendaño, who had held the post since 2006. Ms ...
Results from a pilot project allowing pharmaceutical companies to seek joint scientific advice from the country's drug regulatory authority and its pricing and reimbursement agency are being evaluated 1-3 . The project was conducted to assess ...
The US Food and Drug Administration has announced a review of all its existing drug, medical device, food and tobacco regulations to determine whether they can be made more effective in light of current public health needs and to support advances in ...
A UK parliamentary report has criticised the government's plan to dissolve or merge several public bodies, including many health-related bodies such as the Human Tissue Authority, the Human Fertilisation and Embryology Authority and the Human ...
The EU Council of Ministers has approved new legislation on cross-border healthcare and promoting co-operation on healthcare between member states. The directive 1 , which includes amendments from the European Parliament , will affect the medtech ...
The EU Council of Ministers today approved new legislation on cross-border healthcare and promoting co-operation on healthcare between member states. The directive 1 , which includes amendments from the European Parliament , will affect the ...