Traduction de «patient registration » (Anglais → Français) :

Emergency/Same Day/Daycare Patient Registration

Canadian Forces Cardio-Pulmonary Unit Patient Registration Card

Admissions/Patient Registration

challenge patients' behaviour through art | use art therapy to gently provoke patients | challenge patient behaviour by means of art | challenge patients' behaviour using art

describe the molecular basis of a disease to a patient | explain the metabolic basis of a disease to a patient | explain molecular basis of diseases to patients | explain the molecular basis of a disease to patients

diagnose immunodeficiencies in patients | diagnose patient with immunodeficiencies | diagnose patient with immunodeficiency | diagnose patients with immunodeficiencies

patient's rights [ dignity of patients | patient dignity | rights of patients | rights of the dying | sick person's rights ]

Bite registration rim

Limited access to some areas in the affected countries also complicates the registration and isolation of patients.

Maintain the EU’s coordinative role in the development of the EU policy on rare diseases and to support Member States in their activities on the national level. Continue to support the development of high quality National Rare Diseases Plans/Strategies in the European Union. Provide continued support for the International Rare Disease Research Consortium and initiatives developed under its umbrella. Continue to ensure proper codification of rare diseases. Work further to decrease inequalities between patients with rare diseases and patients suffering from more common disorders and to support initiatives promoting equal access to diagnosi ...[+++]s and treatment. Continue to promote patients empowerment in all aspects of rare diseases policy development Continue activities increasing public awareness about rare diseases and EU activity in this field Make use of the Directive 2011/24/EU on the application of patients’ rights in cross-border healthcare to bring together European Reference Networks on rare diseases. Support the development of the tools facilitating cooperation and interoperability of the European Reference Networks for rare diseases. Stimulate development and use of eHealth solutions in the area of rare diseases. Implement and continue support for the European Platform on rare diseases registration. Continue playing a global role in the rare diseases initiative and collaborating with important international stakeholders.

5. Access criteria shall include a commitment to optimise the use of the clinical trial data through registration of the clinical trial protocol before inclusion of patients in a publicly available registry approved by the World Health Organization (WHO), and through a commitment to report the study results. ECRIN-ERIC shall ensure, once the study is published, access to the raw, anonymised clinical trial data for the scientific community.

Urges the Member States to implement fully the existing Professional Qualifications Directive (2005/36/EC); with regard to the complexity of medical qualifications, encourages the Commission, in its evaluation and review of the directive, to address some of the regulatory gaps that have the potential to leave patients vulnerable to harm and compromise their right to safe treatment; invites the Commission, further, to consider whether to make registration with the IMI System mandatory for competent authorities and improve the extent ...[+++]to which competent authorities can proactively share disciplinary information about healthcare professionals by creating an appropriate alert mechanism;