The medicine development process is complex and requires time and effort to ensure safety, efficacy and quality. In paediatrics, this process is even more challenging, as it involves a subgroup of the population that already faces a considerable gap in the clinical evaluation of medicines and devices compared to the adult population. Moreover, access to therapies is heavily influenced by national health technology assessment (HTA) recommendations, which often form the basis for pricing and reimbursement decisions that affect the effective availability of treatments within the national health systems. Yet performing an HTA to assess the relative effectiveness and cost-effectiveness of a new children’s treatment has several non-trivial implic...
In new legislation for paediatric medicines which came into effect on 26 January 2007, the European ...
drug research for children, but a more focused effort concerning all therapeutic needs is necessary ...
Drug discovery and development advances in the last decades allowed to find a treatment for many pre...
The medicine development process is complex and requires time and effort to ensure safety, efficacy ...
The need for information about new and existing drugs used in children was recognized in the Europea...
Background and aims: There is an alarming delay in Europe for anticancer medicines becoming accessib...
Development of specific medical devices (MDs) is required to meet the healthcare needs of children a...
Development of specific medical devices (MDs) is required to meet the healthcare needs of children a...
Item does not contain fulltextBACKGROUND: It is now widely accepted that there is a need for safety ...
New European legislation has the potential to have an enormous impact on how paediatric medicines ar...
Paediatric clinical trials are critical to ensure that medications prescribed to children are safe a...
Health technology assessment (HTA) is important when launching a new drug or medical device. This th...
Ensuring its success will help improve the use of medicines in children T he importance of clinical ...
Background: As part of the European Paediatric Regulation, the European Medicines Agency (former Eur...
In new legislation for paediatric medicines which came into effect on 26 January 2007, the European ...
drug research for children, but a more focused effort concerning all therapeutic needs is necessary ...
Drug discovery and development advances in the last decades allowed to find a treatment for many pre...
The medicine development process is complex and requires time and effort to ensure safety, efficacy ...
The need for information about new and existing drugs used in children was recognized in the Europea...
Background and aims: There is an alarming delay in Europe for anticancer medicines becoming accessib...
Development of specific medical devices (MDs) is required to meet the healthcare needs of children a...
Development of specific medical devices (MDs) is required to meet the healthcare needs of children a...
Item does not contain fulltextBACKGROUND: It is now widely accepted that there is a need for safety ...
New European legislation has the potential to have an enormous impact on how paediatric medicines ar...
Paediatric clinical trials are critical to ensure that medications prescribed to children are safe a...
Health technology assessment (HTA) is important when launching a new drug or medical device. This th...
Ensuring its success will help improve the use of medicines in children T he importance of clinical ...
Background: As part of the European Paediatric Regulation, the European Medicines Agency (former Eur...
In new legislation for paediatric medicines which came into effect on 26 January 2007, the European ...
drug research for children, but a more focused effort concerning all therapeutic needs is necessary ...
Drug discovery and development advances in the last decades allowed to find a treatment for many pre...