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19 July 2011

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 ...

07 January 2011

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 ...

06 January 2011

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 ...

HTA
19 July 2011

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 ...

12 October 2010

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 ...

27 April 2011

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 ...

11 January 2011

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 ...

01 March 2011

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 ...

28 February 2011

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 ...

 
27 April 2011
Ashley Yeo
With the US in mid-regulatory review, stakeholders are keenly pushing for a safer and faster system, but there are different views on how these goals should be achieved. That was shown at a hearing of the US Senate's Special Committee on Aging 1 . ...
 
09 June 2009
Karen Finn
Nearly a year has elapsed since companies seeking marketing authorisations in the European Union were required to begin submitting paediatric ...
 
01 July 2009
Business compliance is becoming an increasingly important requirement for the pharmaceutical industry. Drug companies are becoming subject to a ...
29 June 2009
Japan?s Pharmaceuticals and Medical Devices Agency is set to undergo a significant change, with its focus shifting towards increased co-operation on ...
09 June 2009
Nearly a year has elapsed since companies seeking marketing authorisations in the European Union were required to begin submitting paediatric ...
 
08 October 2009
Please give details of the major acts and directives governing trademarks. Trademarks are governed in Luxembourg by the: Benelux Convention on ...
08 October 2009
Please give details of the major acts and directives governing trademarks. Trademarks are governed in Luxembourg by the: Benelux Convention on ...
 
RAJ Devices News Roundup, 11 December 2009
28 July 2011
 
Pharmacist takes the helm of Spanish regulator 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 ...
Pharmacist takes the helm of Spain's pharma regulator 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 ...
 
   
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