Übersetzung für "Clinical registry" in Deutsch

A clinical cancer registry is an important part of any tumor center.

Comparable to a clinical trial registry, the new portal is intended to make information on German registries available.

The educational material is aimed to encourage healthcare professionals to enrol patients in the prospective disease and clinical outcome registry of patients with Lysosomal Acid Lipase (LAL) Deficiency to monitor for efficacy and safety of Kanuma (LAL Deficiency Registry), with particular regard to hypersensitivity reactions, including anaphylaxis, and anti-drug antibodies (ADA) development impacting response to drug.

In order to increase transparency in the area of clinical trials, data from a clinical trial should only be submitted in support of a clinical trial application if that clinical trial has been recorded in a publicly accessible and free of charge database which is a primary or partner registry of, or a data provider to, the international clinical trials registry platform of the World Health Organization (WHO ICTRP).

Clinical trial data submitted in an application dossier shall be based on clinical trials which have been registered prior to their start in a public register which is a primary registry of the international clinical trials registry platform of the World Health Organisation.

What is a clinical registry?

The company is now committed to creating both a clinical trial results database to ensure health care providers have ready access to new information and a clinical trial registry to help patients and their physicians find clinical trials that may be appropriate for them.

Both the clinical trial registry and results database, which will be hosted by an independent, neutral entity, will be available to the public via a website by the end of the first quarter 2005.

A week ago we announced that we will be establishing a global clinical trial protocol registry for all our clinical trials (phase II to phase IV) and that by the end of March 2005 we will also be launching a global database disclosing the key results from completed trials.

Health care research uses data from the Clinical Research Cancer Registry or analyzes data together with the Hamburg Cancer Registry.

The clinical trial registry will serve as a global repository for information on ongoing Phase II through Phase IV clinical studies.

WHO International Clinical Trials Registry Platform now available in French, Russian 06-08-2009 The registration of clinical trials enables health care decision-makers to gain a complete view of research, improves research transparency and strengthens the validity and value of the scientific evidence base.

Clinical trials can be registered in free, publicly available, and electronically searchable registers such as ClinicalTrials.gov and the Australian New Zealand Clinical Trial Registry.

Roche announced today that it is establishing a global clinical trial protocol registry to disclose information about new Phase II to Phase IV studies at or before their start.

The clinical trial registry and results database will also include interventional clinical studies from Roche Diagnostics.

The WHO International Clinical Trials Registry Platform is now available in Arabic, Chinese, English, French, Russian and Spanish.

In a close cooperation of physicians, sociologists, medical law experts as well as the Clinical Cancer Registry and the Hamburg Cancer Registry several projects discussing the topic are pursued.

Moreover, as many patients as possible are to be included in clinical studies, a clinical cancer registry must be kept, local self-help organizations must be involved and cooperation with physicians in private practice and hospitals from the surrounding area is to be assured.

Within only three months after deciding to create an electronic database, Roche is launching a public clinical trial registry and results database using an independent host, CenterWatch.

The main tool for this purpose is the Clinical Cancer Registry of the Hubertus Wald Tumor Center, in which information about the treatment quality is gathered in order to develop and proof measures in quality improvement.

If an expert centre, an expert laboratory, a professional, a research project, a clinical trial, a registry, a patient organisation or an institution is not listed for a certain region or country, this could be because Orphanet has not yet identified this information, or because the person in charge has refused to be listed in Orphanet or has not sent back the form they received to fill in.

The network initiates and conducts clinical trials and registries (investigator initiated trials IIT).

Bayer publicly discloses information on its clinical trials by the use of freely accessible Clinical Trial Registries.

The CHMP reviewed all data submitted including data from the French SAGHE study and from clinical trials, registries, cohorts and safety databases (pharmacovigilance) as well as data available in the literature relating to the cardiovascular risk and risk of neoplasm associated with somatropin-treatment.

The CHMP reviewed the available data on the safety of somatropin-containing medicines, including data from clinical trials, registries, and observational studies, as well as reports of side effects from post-marketing surveillance.

Orphanet is a directory of rare diseases, orphan medicines, patient organisations, professionals, expert centres, diagnostic tests, research projects, clinical trials, registries and biobanks.

The integration of several nation-wide clinical registries under the common heading "cystic kidney diseases" will provide the clinical information and the molecular genetics required for valid genotype-phenotype correlation analyses and the search for novel genes.

Public disclosure of clinical trial information is done in line with the position of the global pharmaceutical industry associations laid down in the "Joint Position on the Disclosure of Clinical Trial Information via Clinical Trial Registries and Databases".

Research related resources (research projects, clinical trials, patient registries, biobanks and Variant databases) are also registered in Orphanet database if they are funded by a member agency of the International Rare Diseases Research Consortium (IRDiRC, list of members available here) located in a country for which there is no Orphanet national team.

Research related resources (research projects, clinical trials, patient registries, biobanks and Variant databases) are also collected and registered in Orphanet database if they are funded by a member agency of the International Rare Diseases Research Consortium consortium (IRDiRC, list of members available here) located in a country for which there is no Orphanet national team.

Roche is committed to sharing data from clinical trials and has registered and posted summary reports for trials involving patients on appropriate clinical registries since 2005.

The report describes why governments should take action on e-Health and provides a clear governance structure to oversee implementation, legislation, clinical registries, legal protection and other issues.