Traduction de «fournir des soins prénataux » (Français → Anglais) :

Nothing should prevent the Member State of treatment from also obliging other actors than the healthcare providers, such as insurance providers or public authorities, to provide the information on specific aspects of the healthcare services offered, if that would be more appropriate with regard to the organisation of its healthcare system.

As Elly mentioned before, and as Canada has agreed, the basket includes services such as: access to voluntary family planning information services and commodity, thereby empowering women to voluntarily plan their families and giving them the freedom to decide what method is most appropriate for them; antenatal care, so intermittent prevention of malaria; folic acid and iron; any other tetanus vaccinations; skilled attendance at birth, including emergency obstetrical care—we know that the majority of women are dying during the pregnancy and the childbirthing period—for postpartum hemorrhage, obstructed labour, those issues; immediate postpartum care for the mother and newborn, because most children will die within ...[+++]the first day, or subsequently the first month of life, and then the first year.

This approach includes improving access to antenatal care during pregnancy, improved management of normal delivery by skilled attendants, access to emergency obstetric and neonatal care when needed, and timely postnatal care for both mothers and newborns.

Communication from the Commission of 5 December 2001 - The future of health care and care for the elderly: guaranteeing accessibility, quality and financial viability [COM(2001)723]. This Communication is a response to the conclusions of the Lisbon European Council of March 2000, which stressed that social protection systems needed to be reformed in order to be able to provide high-quality health care services.

In 2012, the project RARECARENET (Information Network on Rare Cancers)[46], which built upon some of previous activities of the Project RARECARE (Surveillance of Rare Cancers in Europe)[47] which provided estimations for incidence, survival, prevalence and mortality for all rare cancers. The project aims (i) to provide updated indicators of rare cancer burden, (ii) to collect and disseminate information on the health care pathways for rare cancers, (iii) to identify the criteria for centres of expertise for rare cancers, (iv) to produce and disseminate information on diagnosis and management of rare cancers, (v) to develop a clinical database on very rare cancers, (vi) to provide new knowledge on these diseases and their clinical management ...[+++], and (vii) to develop and disseminate information for patients including a list of patients’ associations dedicated to rare cancers. In 2013, the European Expert Paediatric Oncology Reference Network for Diagnostics and Treatment (ExPO-r-NeT), to support the provision of healthcare to children and young people with cancer in a Member State other than the Member State of affiliation, when the expertise with certain cancer conditions is rare and case volume low, contributing to provide cross-border best care to rare childhood cancer populations.

In order to provide quality health care, national governments are required to achieve an optimum balance between the health benefits and the cost of medication and treatment.