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lymphoma: A randomized, open label, phase III trial (BELINDA) Document type: Oncology Clinical Trial Protocol EUDRACT number: 2016-002966-29 Version number: 00 (Original Protocol)...
10 Οκτ 2024 · We describe the design of the first large-scale evaluation of an EHR-integrable, patient-facing family history software platform based on the Substitutable Medical Applications and Reusable Technologies on Fast Healthcare Interoperability Resources (SMART on FHIR) standard.
Protocol A written account of all the procedures to be followed in a trial, which describes all the administrative, documentation, analytical and clinical processes used in the trial.
develop clinical research protocols for trials testing an investigational medicinal product (IMP) to be submitted to Swiss authorities. This template is suitable for studies:
3 Φεβ 2014 · Family history is key to the identification of those individuals who have an inherited predisposition to malignancy or who are at increased risk for additional primary cancers.
To draft a sound scientific design of a clinical research study, the medical writer at the TGH, Office of Clinical Research recommends that the following information should be included in a research protocol. It will help facilitate the application submission process and study approval from the Office of Clinical Research and IRB.
• A Handbook for Clinical Investigators Conducting Therapeutic Clinical Trials Supported by CTEP, DCTD, NCI. This resource from the National Cancer Institute covers policies and implementing
