Conférences - Gestion des données cliniques, télésanté

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TOUS LES PAYS (3)
1
Radiomics: Basic Concepts and Clinical Applications for Oncologic Patients
19 avr 2021 - 21 avr 2021 • Barcelona – online, Espagne
Organisateur:
TMC Academy
Résumé:
Today, medical imaging interpretation is solely based on subjective radiological opinions that suffer from increased variability and low reproducibility. Including Radiomics in the diagnostic process is expected to result in the improvement of diagnostic accuracy, as well as the prediction of treatment response and access to valuable early prognosis information. Several modules of the Radiomics pipeline will be presented and discussed starting from the first phase, where a clinician needs to formulate the clinical question. A radiologist will then need to identify the relevant data sources (types of imaging modalities), and after that an imaging scientist should make sure that the data is preprocessed in a way to enable it to be exploited by the next phases in the pipeline. The lesion segmentation should be done by more than one radiologist, and the radiomics features should be computed by an Imaging Scientist in order to proceed to the model training and validation phases made by a Data Scientist.
Contact:
TMC Academy;     Tél.: [935500750];     Email.: academy@telemedicineclinic.com
Identifiant de l'évènement:
1395126
Sujets apparentés:
2
CIRM – Research School — Evolution tumorale, dynamique et statistiques: mathématiques pour données cliniques & expérimentales
05 jul 2021 - 09 jul 2021 • CIRM (Marseille Luminy), France
Organisateur:
CIRM – Centre International de Rencontres Mathématiques
Identifiant de l'évènement:
1312375
3
21 CFR Part 11 - Compliance for Electronic Records and Signatures
29 sep 2022 • online, États-Unis
Organisateur:
compliance4all
Résumé:
Overview:

This Webinar will explain what 21 CFR Part 11 is, why it is important to FDA regulated companies and how conformance to Part 11 differs from just having good IT security.

Procedures for controlling electronic signatures and electronic records as described in the FDA Guidance will be explained.

FDA regulated companies want to transition to electronic records for economy and efficiency. FDA, because of its concern for patient safety, wants to prevent electronic records from being compromised with possible resulting harm to the patient. FDA has set up regulations that address both data security and patient safety. We will show how 21 CFR part 11 considers both.

The confusion over the original FDA regulation and its subsequent "selective enforcement" will be explained. FDA requirements for 21CFR Part 11 validation will be explained. the requirements are composed of technical and procedural aspects. open, closed and hybrid (paper and electronic) systems will be explained.

Contact:
Compliance4all;     Tél.: [8004479407];     Email.: support@compliance4All.com
Identifiant de l'évènement:
1368525
Sujets apparentés:


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Dernière mise à jour: 18 Décembre 2020