Konferenzen zum Thema Klinisches Datenmanagement, E-Health in den Vereinigten Staaten (USA)

Wählen Sie ein Land aus
1
Risk-based Computer System Validation; Reduce Costs and Avoid 483
22. Apr 2020 - 23. Apr 2020 • Virtual Training Through WebEx, Vereinigte Staaten
Veranstalter:
Complianceonline
Zusammenfassung:
This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments. It details the requirements for Part 11 and Annex 11: SOPs, software product features, infrastructure qualification, and validation. The instructor addresses the latest computer system industry standards for data security, data transfer, audit trails, electronic records and signatures, software validation, and computer system validation.
Kontakt:
Tel.: [+1-888-717-2436];     Email: referral@complianceonline.com
Themen:
computer systems validation, computer systems validation training, computer systems validation seminar, csv seminar, computer system validation compliance, computer systems validation regulations, computer systems validation courses, computer systems validation fda, compliance online software training, computer systems validation class room training in the united states
Eintrags-ID:
1345737
Verwandte Fachgebiete:
2
21 CFR Part 11 Compliance for SaaS/Cloud Applications
22. Apr 2020 - 23. Apr 2020 • Virtual Training Through WebEx, Vereinigte Staaten
Veranstalter:
Complianceonline
Zusammenfassung:
This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments. It details the requirements for Part 11 and Annex 11: SOPs, software product features, infrastructure qualification, and validation. The instructor addresses the latest computer system industry standards for data security, data transfer, audit trails, electronic records and signatures, software validation, and computer system validation.
Kontakt:
Tel.: [+1-888-717-2436];     Email: referral@complianceonline.com
Themen:
21 cfr part 11 compliance
Eintrags-ID:
1345681
Verwandte Fachgebiete:
3
Financial Life Cycle of Clinical Research Studies: Best Practice Approaches
21. Mai 2020 - 22. Mai 2020 • Seattle, WA, Vereinigte Staaten
Veranstalter:
Complianceonline
Zusammenfassung:
In the age of technology, many organizations struggle with incorporating federal and billing regulations with electronic systems.
Kontakt:
Tel.: [18887172436];     Email: referral@complianceonline.com
Themen:
Financial management of clinical research, clinical research financial life cycle, clinical trial billing, clinical trial audit, clinical trials billing program, Financial Management of Clinical Trials, patient billing
Eintrags-ID:
1324709
4
Analytical Instrument Qualification and System Validation
17. Sep 2020 - 18. Sep 2020 • Philadelphia, PA, Vereinigte Staaten
Veranstalter:
Complianceonline
Zusammenfassung:
Analytical equipment should be qualified, and computer systems should be validated to demonstrate suitability for their intended use. To be acceptable to regulatory authorities, electronic records must comply with 21 CFR Part 11, Annex 11 to EU GMPs and more recent data integrity guidance. Recent EU and FDA reports demonstrate that qualification, validation and electronic records are priority areas for inspection. The large number of FDA warning letters and the frequency of EU enforcement action in these areas demonstrate that companies sometimes struggle to understand or implement the regulations. This 2-day course guides attendees through equipment qualification, calibration and computer system validation processes from planning to reporting. It also explains regulatory requirements in these areas, including EU and US GMPs, as well as data integrity guidance documents from national and international regulatory bodies. The course not only ensures a full understanding of the regulations and guidelines for equipment and records but helps attendees to develop a risk-based approach to compliance. Interactive exercises will be dispersed into and between the presentations.
Kontakt:
Tel.: [+1-888-717-2436];     Email: referral@complianceonline.com
Themen:
Computer System Validation seminar, USP <1058>, GAMP 5, equipment calibration, system validation, qualification and validation strategy, archive raw data from hybrid systems, Analytical Instrument Qualification, USP General Chapter <1058>, instrument qualification lifecycle, 21 CFR Part 211, Part 11, PIC/S, EU Annex 11, GMP Computer Systems, Laboratory Computerized Systems, Use of Excel in QC Laboratory, revalidation of chromatography, data security and integrity issues
Eintrags-ID:
1345691
5
AMIA 2020 — AMIA 2020 Annual Symposium
14. Nov 2020 - 18. Nov 2020 • Chicago, Vereinigte Staaten
Zusammenfassung:
We invite you to contribute your best work for presentation at the AMIA 2020 Annual Symposium – the foremost symposium for the science and practice of biomedical informatics.
Eintrags-ID:
1331051


Conference-Service.com stellt der Öffentlichkeit ein Kalendarium wichtiger Konferenzen, Symposien und sonstiger Tagungen im wissenschaftlich-technischen Bereich zur Verfügung. Obwohl das Verzeichnis mit großer Sorgfalt zusammengestellt und ständig aktualisiert wird, weisen wir auf die Möglichkeit von Fehlern ausdrücklich hin. Bitte vergewissern Sie sich immer beim Veranstalter, bevor Sie über die Teilnahme oder Nichtteilnahme an einer Konferenz entscheiden.

Stand vom 03. April 2020