Conferences and Meetings on Clinical Data Management, e-Health

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Radiomics: Basic Concepts and Clinical Applications for Oncologic Patients
19 Apr 2021 - 21 Apr 2021 • Barcelona – online, Spain
TMC Academy
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.
TMC Academy;     Phone: [935500750];     Email:
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CIRM – Research School — Dynamics and Statistics of Cancer Evolution : Applying Mathematics to Experimental and Clinical Data
05 Jul 2021 - 09 Jul 2021 • CIRM (Marseille Luminy), France
CIRM – Centre International de Rencontres Mathématiques
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21 CFR Part 11 - Compliance for Electronic Records and Signatures
29 Sep 2022 • online, United States

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.

Compliance4all;     Phone: [8004479407];     Email:
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Related subject(s): offers, as part of its business activities, a directory of upcoming scientific and technical meetings. The calendar is published for the convenience of conference participants and we strive to support conference organisers who need to publish their upcoming events. Although great care is being taken to ensure the correctness of all entries, we cannot accept any liability that may arise from the presence, absence or incorrectness of any particular information on this website. Always check with the meeting organiser before making arrangements to participate in an event!

Last updated: 18 December 2020